DD238046A5 - Verfahren zur herstellung von alkylenoxiden aus alkylencarbonaten - Google Patents

Verfahren zur herstellung von alkylenoxiden aus alkylencarbonaten Download PDF

Info

Publication number: DD238046A5
Authority: DD; German Democratic Republic
Prior art keywords: alkylene; quaternary; carbonate; ethylene; reaction
Prior art date: 1984-10-25

Application number

DD85282037A

Other languages

German (de)

English (en)

Inventor

Robert M Weinstein

Original Assignee

��@��@��@��K@��Kk��

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-10-25

Filing date

1985-10-24

Publication date

1986-08-06

1985-10-24 Application filed by ��@��@��@��K@��Kk�� filed Critical ��@��@��@��K@��Kk��

1986-08-06 Publication of DD238046A5 publication Critical patent/DD238046A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 21
238000002360 preparation method Methods 0.000 title abstract description 4
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 title description 3
-1 alkylene carbonate Chemical compound 0.000 claims abstract description 46
125000002947 alkylene group Chemical group 0.000 claims abstract description 13
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 5
125000003342 alkenyl group Chemical group 0.000 claims abstract description 5
125000000217 alkyl group Chemical group 0.000 claims abstract description 5
125000003118 aryl group Chemical group 0.000 claims abstract description 5
125000000392 cycloalkenyl group Chemical group 0.000 claims abstract description 5
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 5
239000001257 hydrogen Substances 0.000 claims abstract description 5
125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 5
239000011630 iodine Substances 0.000 claims abstract description 5
229910052740 iodine Inorganic materials 0.000 claims abstract description 5
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 24
KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical group O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 23
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 17
239000001569 carbon dioxide Substances 0.000 claims description 12
229910002092 carbon dioxide Inorganic materials 0.000 claims description 12
238000004519 manufacturing process Methods 0.000 claims description 9
NTIVEBOPRSMRSY-UHFFFAOYSA-M tetraphenylarsanium;iodide Chemical group [I-].C1=CC=CC=C1[As+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 NTIVEBOPRSMRSY-UHFFFAOYSA-M 0.000 claims description 9
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
125000001246 bromo group Chemical group Br* 0.000 abstract 1
125000001309 chloro group Chemical group Cl* 0.000 abstract 1
239000003054 catalyst Substances 0.000 description 22
238000006243 chemical reaction Methods 0.000 description 15
238000000354 decomposition reaction Methods 0.000 description 14
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 12
238000002474 experimental method Methods 0.000 description 6
150000002924 oxiranes Chemical class 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
239000007795 chemical reaction product Substances 0.000 description 4
RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 4
PTBXOARBTPRBHN-UHFFFAOYSA-N 4-oxo-7h-thieno[2,3-b]pyridine-5-carboxylic acid Chemical compound O=C1C(C(=O)O)=CNC2=C1C=CS2 PTBXOARBTPRBHN-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
150000004649 carbonic acid derivatives Chemical class 0.000 description 3
238000004817 gas chromatography Methods 0.000 description 3
229930195733 hydrocarbon Natural products 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
229910001508 alkali metal halide Inorganic materials 0.000 description 2
150000008045 alkali metal halides Chemical class 0.000 description 2
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
229910052787 antimony Inorganic materials 0.000 description 2
VUEDNLCYHKSELL-UHFFFAOYSA-N arsonium Chemical class [AsH4+] VUEDNLCYHKSELL-UHFFFAOYSA-N 0.000 description 2
238000009835 boiling Methods 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
239000007789 gas Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
GHLKOMSNOFJXDT-UHFFFAOYSA-M methyl(triphenyl)arsanium;iodide Chemical compound [I-].C=1C=CC=CC=1[As+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 GHLKOMSNOFJXDT-UHFFFAOYSA-M 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
235000011121 sodium hydroxide Nutrition 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
239000011701 zinc Chemical class 0.000 description 2
229910052725 zinc Chemical class 0.000 description 2
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical class [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
ZQRVHOSWIMRCOI-UHFFFAOYSA-N [AsH2]C(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1.Br Chemical compound [AsH2]C(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1.Br ZQRVHOSWIMRCOI-UHFFFAOYSA-N 0.000 description 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
239000001099 ammonium carbonate Substances 0.000 description 1
235000011162 ammonium carbonates Nutrition 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
PDGPVQHGCLPCES-UHFFFAOYSA-L dichloro(triphenyl)-$l^{5}-stibane Chemical compound C=1C=CC=CC=1[Sb](Cl)(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 PDGPVQHGCLPCES-UHFFFAOYSA-L 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
231100001261 hazardous Toxicity 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
KYKBXWMMXCGRBA-UHFFFAOYSA-K lanthanum(3+);triiodide Chemical class I[La](I)I KYKBXWMMXCGRBA-UHFFFAOYSA-K 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Chemical class 0.000 description 1
239000000203 mixture Substances 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
238000003408 phase transfer catalysis Methods 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000005070 sampling Methods 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
239000013589 supplement Substances 0.000 description 1
BKYRQHURQDNECO-UHFFFAOYSA-M tetrabutylarsanium;iodide Chemical compound [I-].CCCC[As+](CCCC)(CCCC)CCCC BKYRQHURQDNECO-UHFFFAOYSA-M 0.000 description 1
KEFJVVFCFZNVQM-UHFFFAOYSA-M tetramethylarsanium;iodide Chemical compound [I-].C[As+](C)(C)C KEFJVVFCFZNVQM-UHFFFAOYSA-M 0.000 description 1
IUVXCVGGLRYGFE-UHFFFAOYSA-N tetraphenyl-lambda5-arsane hydrochloride Chemical compound C1=CC=C(C=C1)[AsH](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.Cl IUVXCVGGLRYGFE-UHFFFAOYSA-N 0.000 description 1
NZUQEBQRKNZZDO-UHFFFAOYSA-M tetraphenylarsanium;bromide Chemical compound [Br-].C1=CC=CC=C1[As+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 NZUQEBQRKNZZDO-UHFFFAOYSA-M 0.000 description 1
NGDWSDTZKCSLRK-UHFFFAOYSA-M tetraphenylarsanium;chloride;hydrate Chemical compound O.[Cl-].C1=CC=CC=C1[As+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 NGDWSDTZKCSLRK-UHFFFAOYSA-M 0.000 description 1
239000011135 tin Chemical class 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
IZYFBZDLXRHRLF-UHFFFAOYSA-N tritylphosphane;hydroiodide Chemical compound [I-].C=1C=CC=CC=1C(C=1C=CC=CC=1)([PH3+])C1=CC=CC=C1 IZYFBZDLXRHRLF-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Catalysts (AREA)
Epoxy Compounds (AREA)

DD85282037A 1984-10-25 1985-10-24 Verfahren zur herstellung von alkylenoxiden aus alkylencarbonaten DD238046A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/664,728 US4851555A (en)	1984-10-25	1984-10-25	Process for preparing alkylene oxides from alkylene carbonates

Publications (1)

Publication Number	Publication Date
DD238046A5 true DD238046A5 (de)	1986-08-06

Family

ID=24667217

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85282037A DD238046A5 (de)	1984-10-25	1985-10-24	Verfahren zur herstellung von alkylenoxiden aus alkylencarbonaten

Country Status (18)

Country	Link
US (1)	US4851555A (fr)
EP (1)	EP0180387B1 (fr)
JP (1)	JPS61103878A (fr)
KR (1)	KR860003235A (fr)
CN (1)	CN1007152B (fr)
AR (1)	AR241245A1 (fr)
AU (1)	AU577629B2 (fr)
BG (1)	BG48458A3 (fr)
BR (1)	BR8505283A (fr)
CA (1)	CA1238643A (fr)
DD (1)	DD238046A5 (fr)
DE (1)	DE3577557D1 (fr)
ES (1)	ES8606317A1 (fr)
IN (1)	IN164704B (fr)
RO (1)	RO93390B (fr)
SU (1)	SU1648251A3 (fr)
YU (1)	YU45925B (fr)
ZA (1)	ZA858221B (fr)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4030283A1 (de) *	1990-09-25	1992-03-26	Ruetgerswerke Ag	Verfahren zur herstellung cyclischer carbonate
DE4105554A1 (de)	1991-02-22	1992-08-27	Bayer Ag	Verfahren zur herstellung von dialkylcarbonaten
JP3098934B2 (ja) *	1995-06-06	2000-10-16	矢崎総業株式会社	コネクタ
FR2760747B1 (fr)	1997-03-12	1999-06-04	Organisation Nationale Interpr	Procede de fabrication de glycidol ou d'un compose glycidyle
US5902894A (en)	1998-08-26	1999-05-11	Catalytic Distillation Technologies	Process for making dialkyl carbonates
US6258962B1 (en)	1999-06-14	2001-07-10	Mobil Oil Corp.	Process for producing alkylene carbonates
US6407279B1 (en)	1999-11-19	2002-06-18	Exxonmobil Chemical Patents Inc.	Integrated process for preparing dialkyl carbonates and diols
US7378540B2 (en) *	2005-10-21	2008-05-27	Catalytic Distillation Technologies	Process for producing organic carbonates
TWI382979B (zh)	2006-02-22	2013-01-21	Shell Int Research	碳酸伸烷酯之生產方法及由此生產的碳酸伸烷酯於烷二醇及碳酸二烷酯之製造中的用途
TWI383976B (zh)	2006-02-22	2013-02-01	Shell Int Research	製備碳酸二烷酯及烷二醇的方法
TWI378087B (en)	2006-02-22	2012-12-01	Shell Int Research	Process for the preparation of an alkanediol and a dialkyl carbonate
TW200740731A (en)	2006-02-22	2007-11-01	Shell Int Research	Process for the preparation of alkanediol
EP2121566B1 (fr)	2007-01-23	2012-10-31	Shell Internationale Research Maatschappij B.V.	Procédé de préparation d'un alcanediol et d'un carbonate de dialkyle
US7732630B2 (en)	2007-01-23	2010-06-08	Shell Oil Company	Process for the preparation of an alkanediol and a dialkyl carbonate
ES2442744T3 (es)	2008-10-20	2014-02-13	Shell Internationale Research Maatschappij B.V.	Procedimiento para eliminar una impureza de alcanol de una corriente de carbonato orgánico
DE102009030680A1 (de)	2009-06-26	2010-12-30	Bayer Materialscience Ag	Verfahren zur Herstellung von Dialkylcarbonaten aus Alkylencarbonaten und Alkoholen
TWI511953B (zh)	2009-08-12	2015-12-11	Shell Int Research	自碳酸二烷酯流移除烷醇不純物的方法
US8618322B2 (en)	2009-09-29	2013-12-31	Shell Oil Company	Process for preparing alkanediol and dialkyl carbonate
DE102009053370A1 (de)	2009-11-14	2011-05-19	Bayer Materialscience Ag	Verfahren zur Reinigung von Dialkylcarbonaten
TWI473786B (zh)	2009-11-16	2015-02-21	Shell Int Research	製備烷二醇及碳酸二烷酯的方法
DE102010006657A1 (de)	2010-02-03	2011-08-04	Bayer MaterialScience AG, 51373	Verfahren zur Herstellung von Dialkylcarbonaten
DE102010042937A1 (de)	2010-10-08	2012-04-12	Bayer Materialscience Aktiengesellschaft	Verfahren zur Herstellung von Diarylcarbonaten aus Dialkylcarbonaten
EP2650278A1 (fr)	2012-04-11	2013-10-16	Bayer MaterialScience AG	Procédé de fabrication de diarylcarbonates à partir de dialkylcarbonates
EP2922810B1 (fr)	2012-11-21	2016-12-21	Covestro Deutschland AG	Procédé de préparation de carbonates de dialkyle
WO2019016126A1 (fr)	2017-07-18	2019-01-24	Shell Internationale Research Maatschappij B.V.	Procédé de préparation d'alcanediol et de carbonate de dialkyle
CN110156723B (zh) *	2018-02-13	2021-05-07	中国科学院过程工程研究所	1, 2-环氧化合物的合成方法
ES2972157T3 (es)	2018-12-18	2024-06-11	Shell Int Research	Proceso para preparar carbonato de dialquilo y alcanodiol
CN110078685B (zh) *	2019-04-19	2021-03-02	中国科学院过程工程研究所	一种连续反应制备环氧化合物的装置及方法
CN110156724B (zh) *	2019-04-19	2021-03-09	中国科学院过程工程研究所	一种间歇反应制备环氧化合物的装置及方法
US12098125B2 (en)	2019-10-03	2024-09-24	Shell Usa, Inc.	Process for preparing dialkyl carbonate and alkanediol
WO2021110627A1 (fr)	2019-12-06	2021-06-10	Shell Internationale Research Maatschappij B.V.	Procédé pour l'élimination d'une impureté d'alcanol éther à partir d'un flux de carbonate organique
EP3831805A1 (fr)	2019-12-06	2021-06-09	Shell Internationale Research Maatschappij B.V.	Procédé de préparation d'un carbonate de dialkyle et d'un alcanédiol
IT202000022624A1 (it)	2020-09-24	2022-03-24	Milano Politecnico	Processo di produzione di alchilene ossidi da alchilencarbonati

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2851469A (en) *		1958-09-09		Manufacture of ethylene oxide
US2994704A (en) *	1958-11-19	1961-08-01	Pure Oil Co	Preparation of cyclic alkylene carbonates
US4069234A (en) *	1974-04-10	1978-01-17	Phillips Petroleum Company	Preparation of vicinal epoxides
US4192810A (en) *	1974-04-10	1980-03-11	Phillips Petroleum Company	Preparation of vicinal epoxides
US3923842A (en) *	1974-06-28	1975-12-02	Phillips Petroleum Co	Preparation of oxirane compound from the corresponding olefin via the cyclic carbonate ester
IT1095606B (it) *	1978-04-14	1985-08-10	Montedison Spa	Processo per la sintesi di alchilencarbonati
US4265821A (en) *	1978-06-29	1981-05-05	Texaco Dev. Corp.	Substituted alkylene oxides from substituted alkylene carbonates
US4374259A (en) *	1978-06-29	1983-02-15	Texaco Development Corporation	Process for converting substituted ethylene carbonates into substituted ethylene oxides using tin catalysts
US4371704A (en) *	1978-06-29	1983-02-01	Texaco Development Corporation	Substituted alkylene oxides from substituted alkylene carbonates
US4257966A (en) *	1978-08-17	1981-03-24	Phillips Petroleum Company	Preparation of vicinal epoxides
JPS55122776A (en) *	1979-03-14	1980-09-20	Harukazu Matsuda	Synthetic method of carbonate
US4276223A (en) *	1979-09-10	1981-06-30	Phillips Petroleum Company	Preparation of vicinal epoxides
CA1168252A (fr) *	1980-09-04	1984-05-29	Union Carbide Corporation	Procede d'obtention d'epoxydes a partir de carbonates d'alkylene
CA1162199A (fr) *	1980-09-04	1984-02-14	Charles H. Mcmullen	Methode de preparation d'epoxydes a partir de carbonates d'alkylene
US4345984A (en) *	1981-03-02	1982-08-24	The Procter & Gamble Company	Novel prostaglandin analogues and process for making same
IN159117B (fr) *	1981-12-02	1987-03-28	Halcon Sd Group Inc

1984
- 1984-10-25 US US06/664,728 patent/US4851555A/en not_active Expired - Fee Related
1985
- 1985-09-13 IN IN754/DEL/85A patent/IN164704B/en unknown
- 1985-09-18 CA CA000491058A patent/CA1238643A/fr not_active Expired
- 1985-10-07 JP JP60223448A patent/JPS61103878A/ja active Pending
- 1985-10-15 AR AR85301962A patent/AR241245A1/es active
- 1985-10-18 DE DE8585307550T patent/DE3577557D1/de not_active Expired - Fee Related
- 1985-10-18 AU AU48839/85A patent/AU577629B2/en not_active Ceased
- 1985-10-18 EP EP85307550A patent/EP0180387B1/fr not_active Expired - Lifetime
- 1985-10-23 BR BR8505283A patent/BR8505283A/pt unknown
- 1985-10-24 CN CN85108659A patent/CN1007152B/zh not_active Expired
- 1985-10-24 DD DD85282037A patent/DD238046A5/de not_active IP Right Cessation
- 1985-10-24 KR KR1019850007856A patent/KR860003235A/ko not_active Ceased
- 1985-10-24 SU SU853969751A patent/SU1648251A3/ru active
- 1985-10-24 YU YU168785A patent/YU45925B/sh unknown
- 1985-10-24 ES ES548180A patent/ES8606317A1/es not_active Expired
- 1985-10-25 ZA ZA858221A patent/ZA858221B/xx unknown
- 1985-10-25 BG BG072148A patent/BG48458A3/xx unknown
- 1985-10-25 RO RO120545A patent/RO93390B/ro unknown

Also Published As

Publication number	Publication date
IN164704B (fr)	1989-05-13
CA1238643A (fr)	1988-06-28
JPS61103878A (ja)	1986-05-22
YU168785A (en)	1987-12-31
ES548180A0 (es)	1986-04-01
AU4883985A (en)	1986-05-01
CN1007152B (zh)	1990-03-14
BR8505283A (pt)	1986-08-05
RO93390B (ro)	1988-01-01
CN85108659A (zh)	1986-07-16
EP0180387A2 (fr)	1986-05-07
AR241245A1 (es)	1992-03-31
KR860003235A (ko)	1986-05-21
EP0180387B1 (fr)	1990-05-09
RO93390A (fr)	1987-12-31
EP0180387A3 (en)	1987-05-13
AU577629B2 (en)	1988-09-29
US4851555A (en)	1989-07-25
SU1648251A3 (ru)	1991-05-07
ZA858221B (en)	1987-06-24
BG48458A3 (en)	1991-02-15
DE3577557D1 (de)	1990-06-13
ES8606317A1 (es)	1986-04-01
YU45925B (sh)	1992-09-07

Legal Events

Date	Code	Title	Description
1997-07-17	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DD238046A5 (de)	1986-08-06	Verfahren zur herstellung von alkylenoxiden aus alkylencarbonaten
DE69102826T3 (de)	1998-08-27	Verfahren zur Herstellung von Dimethylcarbonat.
EP0499924B1 (fr)	1994-10-05	Procédé de préparation de carbonates de dialkyle
DE69223367T2 (de)	1998-05-14	Verfahren zur Herstellung von Alkylcarbonaten
DE4129316A1 (de)	1993-03-04	Verfahren zur kontinuierlichen herstellung von dialkylcarbonaten
DE2937956A1 (de)	1980-11-27	Verfahren zur herstellung von alkylenglykolen
EP0654461A1 (fr)	1995-05-24	Procédé de préparation de carbonates de diaryle
EP0413215B1 (fr)	1994-04-20	Procédé de préparation de carbonates de dialkyle
EP0041622A1 (fr)	1981-12-16	Procédé de préparation de carbonates
DE69328056T2 (de)	2000-10-05	Verfahren zur Herstellung von Alkylen-Karbonaten
EP0523508B1 (fr)	1995-09-13	Procédé de fabrication de carbonates de dialkyle
DE2340395C3 (de)	1982-05-27	Verfahren zur Herstellung von vicinalen Glykolestern
DE69012209T2 (de)	1994-12-22	Ethylbenzol-Oxidation.
DE2531166C2 (de)	1983-05-26	Verfahren zur Herstellung von 1,5,9-Cyclododecatrien
DE602004012344T2 (de)	2009-03-12	Verfahren zur Herstellung von Alkylenglykolen unter Verwendung von homogenen Katalysatoren
DE69205601T2 (de)	1996-04-11	Verfahren zur Herstellung von 3-Cyano-3,5,5-trimethylcyclohexanon.
EP0736511A1 (fr)	1996-10-09	Procédé de préparation de carbonates de diaryl
DE60001151T2 (de)	2003-08-21	Lösungsmittelfreies verfahren zur herstellung von thiuram-disulfiden
DE3816932A1 (de)	1989-02-02	Verfahren zur herstellung von hexafluoraceton und seines hydrates
DE69319343T2 (de)	1999-03-25	Verfahren zur herstellung von adipinsäure
DE3504732A1 (de)	1985-08-29	Verfahren zur herstellung eines gemisches von phosphornitridchlorid-oligomeren
DE3151336A1 (de)	1982-07-22	Verfahren zur herstellung von ethylidendiacetat
DE3030842C2 (de)	1984-07-12	Verfahren zur Herstellung von Kohlenmonoxid
DE3031289A1 (de)	1981-03-12	Verfahren zur herstellung von alkylencarbonaten.
DE3121180A1 (de)	1982-02-04	Verfahren zur herstellung von mono- oder poly-alkylen-glykol-diaethern