DD207900A5 - Verfahren zur karbonylierung von olefinen und organischen estern - Google Patents

Verfahren zur karbonylierung von olefinen und organischen estern Download PDF

Info

Publication number: DD207900A5
Authority: DD; German Democratic Republic
Prior art keywords: carbon monoxide; organic compound; acid; reactor; item
Prior art date: 1981-07-10

Application number

DD82240468A

Other languages

German (de)

English (en)

Inventor

John E Corn

Richard V Norton

Ralph F Pascoe

Original Assignee

Ashland Oil Inc

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.)

1981-07-10

Filing date

1982-06-04

Publication date

1984-03-21

1982-06-04 Application filed by Ashland Oil Inc filed Critical Ashland Oil Inc

1984-03-21 Publication of DD207900A5 publication Critical patent/DD207900A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 35
150000001336 alkenes Chemical class 0.000 title claims abstract description 14
150000002895 organic esters Chemical class 0.000 title claims abstract description 8
229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 79
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 75
239000002253 acid Substances 0.000 claims abstract description 50
150000002894 organic compounds Chemical class 0.000 claims abstract description 39
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 33
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
230000006315 carbonylation Effects 0.000 claims abstract description 4
238000005810 carbonylation reaction Methods 0.000 claims abstract description 4
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 37
150000001450 anions Chemical class 0.000 claims description 32
229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 31
239000000203 mixture Substances 0.000 claims description 24
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 19
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 15
230000015572 biosynthetic process Effects 0.000 claims description 9
125000004432 carbon atom Chemical group C* 0.000 claims description 7
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 7
WVRPFQGZHKZCEB-UHFFFAOYSA-N Isopropyl 2-methylpropanoate Chemical compound CC(C)OC(=O)C(C)C WVRPFQGZHKZCEB-UHFFFAOYSA-N 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 claims description 5
WDAXFOBOLVPGLV-UHFFFAOYSA-N ethyl isobutyrate Chemical compound CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 claims description 4
229940024423 isopropyl isobutyrate Drugs 0.000 claims description 4
IJMWOMHMDSDKGK-UHFFFAOYSA-N Isopropyl propionate Chemical compound CCC(=O)OC(C)C IJMWOMHMDSDKGK-UHFFFAOYSA-N 0.000 claims description 3
239000011541 reaction mixture Substances 0.000 claims description 3
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
239000005977 Ethylene Substances 0.000 claims description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 2
208000011130 pituitary stalk interruption syndrome Diseases 0.000 claims description 2
LEMQFBIYMVUIIG-UHFFFAOYSA-N trifluoroborane;hydrofluoride Chemical compound F.FB(F)F LEMQFBIYMVUIIG-UHFFFAOYSA-N 0.000 claims 1
FSQOYWQCIXSBNP-UHFFFAOYSA-N 2-methylpropanoyl fluoride Chemical compound CC(C)C(F)=O FSQOYWQCIXSBNP-UHFFFAOYSA-N 0.000 abstract description 15
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract description 5
238000004519 manufacturing process Methods 0.000 abstract description 3
230000002427 irreversible effect Effects 0.000 abstract description 2
VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 abstract description 2
238000006116 polymerization reaction Methods 0.000 abstract description 2
238000006243 chemical reaction Methods 0.000 description 42
239000000047 product Substances 0.000 description 39
239000007791 liquid phase Substances 0.000 description 15
150000008065 acid anhydrides Chemical class 0.000 description 14
238000002156 mixing Methods 0.000 description 12
150000001732 carboxylic acid derivatives Chemical class 0.000 description 11
239000007788 liquid Substances 0.000 description 11
-1 carbon monoxide Compound Chemical class 0.000 description 10
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 10
238000005886 esterification reaction Methods 0.000 description 9
238000004821 distillation Methods 0.000 description 8
230000032050 esterification Effects 0.000 description 8
238000006460 hydrolysis reaction Methods 0.000 description 8
150000002148 esters Chemical class 0.000 description 7
230000007062 hydrolysis Effects 0.000 description 7
239000000376 reactant Substances 0.000 description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
150000001733 carboxylic acid esters Chemical class 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
239000012071 phase Substances 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
239000007789 gas Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
230000035484 reaction time Effects 0.000 description 3
239000000126 substance Substances 0.000 description 3
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
239000003153 chemical reaction reagent Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
230000008021 deposition Effects 0.000 description 2
238000010586 diagram Methods 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
238000000926 separation method Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
229910000792 Monel Inorganic materials 0.000 description 1
150000001265 acyl fluorides Chemical class 0.000 description 1
238000013019 agitation Methods 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
QGGYSAJKSPQZHU-UHFFFAOYSA-N carbon monoxide hydrofluoride Chemical compound [C]=O.F QGGYSAJKSPQZHU-UHFFFAOYSA-N 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003245 coal Substances 0.000 description 1
239000000567 combustion gas Substances 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
150000002222 fluorine compounds Chemical class 0.000 description 1
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
CUPFNGOKRMWUOO-UHFFFAOYSA-N hydron;difluoride Chemical compound F.F CUPFNGOKRMWUOO-UHFFFAOYSA-N 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
WMFABESKCHGSRC-UHFFFAOYSA-N propanoyl fluoride Chemical compound CCC(F)=O WMFABESKCHGSRC-UHFFFAOYSA-N 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000008929 regeneration Effects 0.000 description 1
238000011069 regeneration method Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000012808 vapor phase Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/04—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid halides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/12—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/14—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on a carbon-to-carbon unsaturated bond in organic compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD82240468A 1981-07-10 1982-06-04 Verfahren zur karbonylierung von olefinen und organischen estern DD207900A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US28213081A	1981-07-10	1981-07-10

Publications (1)

Publication Number	Publication Date
DD207900A5 true DD207900A5 (de)	1984-03-21

Family

ID=23080232

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82240468A DD207900A5 (de)	1981-07-10	1982-06-04	Verfahren zur karbonylierung von olefinen und organischen estern

Country Status (19)

Country	Link
JP (1)	JPS6024089B2 (fr)
KR (1)	KR850001912B1 (fr)
AT (1)	AT392066B (fr)
AU (1)	AU532911B1 (fr)
BE (1)	BE893415A (fr)
BR (1)	BR8203330A (fr)
CA (1)	CA1192576A (fr)
CH (1)	CH656608A5 (fr)
DD (1)	DD207900A5 (fr)
DE (1)	DE3221173C2 (fr)
ES (2)	ES8400376A1 (fr)
FR (1)	FR2512811B1 (fr)
GB (1)	GB2101591B (fr)
IT (1)	IT1195931B (fr)
NL (1)	NL187626C (fr)
PL (1)	PL140231B1 (fr)
RO (1)	RO83931B (fr)
SE (1)	SE452609B (fr)
ZA (1)	ZA823929B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0759531B2 (ja) *	1986-11-04	1995-06-28	三菱瓦斯化学株式会社	フツ化イソブチリルの合成方法
US5463095A (en) *	1993-06-15	1995-10-31	Mitsubishi Gas Chemical Company, Inc.	Process for the production of esters
BR102012020205A2 (pt) *	2012-08-13	2014-08-19	Cesar Roque Ecker	Aplicador de argamassa

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE972291C (de) *	1954-05-16	1959-07-02	Studiengesellschaft Kohle Mbh	Verfahren zur Herstellung von Monocarbonsaeuren aus Olefinen, Kohlenoxyd und Wasser
DE973077C (de) *	1954-07-30	1959-11-26	Studiengesellschaft Kohle Mbh	Verfahren zur Herstellung von Carbonsaeuren aus Olefinen und Kohlenoxyd
DE1064941B (de) *	1957-04-24	1959-09-10	Studiengesellschaft Kohle Mbh	Verfahren zur Herstellung von Gemischen aus gesaettigten aliphatischen oder cycloaliphatischen Monocarbonsaeurealkylestern
US3065242A (en) *	1960-02-23	1962-11-20	Du Pont	Production of acyl halides, carboxylic acids and lactones
GB942367A (en) *	1961-04-29	1963-11-20	Basf Ag	Continuous production of carboxylic acids from olefines, carbon monoxide and water
NL6816940A (fr) *	1967-11-28	1969-05-30
BE755997A (fr) *	1969-09-11	1971-03-10	Bp Chem Int Ltd	Production d'acides dicarboxyliques
DE2750719A1 (de) *	1977-11-12	1979-05-17	Roehm Gmbh	Verfahren zur herstellung von isobuttersaeure

1982
- 1982-06-04 RO RO107796A patent/RO83931B/ro unknown
- 1982-06-04 ES ES513956A patent/ES8400376A1/es not_active Expired
- 1982-06-04 DE DE3221173A patent/DE3221173C2/de not_active Expired
- 1982-06-04 AU AU84608/82A patent/AU532911B1/en not_active Ceased
- 1982-06-04 BE BE0/208267A patent/BE893415A/fr not_active IP Right Cessation
- 1982-06-04 GB GB08216302A patent/GB2101591B/en not_active Expired
- 1982-06-04 DD DD82240468A patent/DD207900A5/de not_active IP Right Cessation
- 1982-06-04 CA CA000404491A patent/CA1192576A/fr not_active Expired
- 1982-06-04 FR FR8209811A patent/FR2512811B1/fr not_active Expired
- 1982-06-04 AT AT0217782A patent/AT392066B/de not_active IP Right Cessation
- 1982-06-04 CH CH3477/82A patent/CH656608A5/de not_active IP Right Cessation
- 1982-06-04 IT IT21709/82A patent/IT1195931B/it active
- 1982-06-04 NL NLAANVRAGE8202269,A patent/NL187626C/xx not_active IP Right Cessation
- 1982-06-04 ZA ZA823929A patent/ZA823929B/xx unknown
- 1982-06-04 SE SE8203478A patent/SE452609B/sv not_active IP Right Cessation
- 1982-06-04 KR KR8202508A patent/KR850001912B1/ko not_active Expired
- 1982-06-04 PL PL1982236785A patent/PL140231B1/pl unknown
- 1982-06-04 JP JP57096066A patent/JPS6024089B2/ja not_active Expired
- 1982-06-07 BR BR8203330A patent/BR8203330A/pt not_active IP Right Cessation
1983
- 1983-06-01 ES ES523258A patent/ES523258A0/es active Granted

Also Published As

Publication number	Publication date
NL8202269A (nl)	1983-02-01
IT1195931B (it)	1988-11-03
IT8221709A0 (it)	1982-06-04
ES513956A0 (es)	1983-10-16
PL236785A1 (en)	1983-02-14
ES8500208A1 (es)	1984-10-01
JPS5810535A (ja)	1983-01-21
BE893415A (fr)	1982-10-01
PL140231B1 (en)	1987-04-30
NL187626B (nl)	1991-07-01
SE8203478L (sv)	1983-01-11
DE3221173C2 (de)	1984-07-26
BR8203330A (pt)	1983-05-24
AT392066B (de)	1991-01-25
RO83931A (fr)	1984-04-12
ZA823929B (en)	1983-11-30
NL187626C (nl)	1991-12-02
FR2512811B1 (fr)	1985-07-05
GB2101591B (en)	1985-11-27
JPS6024089B2 (ja)	1985-06-11
CA1192576A (fr)	1985-08-27
ES523258A0 (es)	1984-10-01
ES8400376A1 (es)	1983-10-16
RO83931B (ro)	1984-05-30
ATA217782A (de)	1990-07-15
KR840000464A (ko)	1984-02-22
CH656608A5 (de)	1986-07-15
AU532911B1 (en)	1983-10-20
FR2512811A1 (fr)	1983-03-18
DE3221173A1 (de)	1983-01-27
SE452609B (sv)	1987-12-07
GB2101591A (en)	1983-01-19
KR850001912B1 (ko)	1985-12-31

Legal Events

Date	Code	Title	Description
1994-09-29	ENJ	Ceased due to non-payment of renewal fee

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DE69716860T2 (de)	2003-07-31	Iridium katalysiertes Carbonylierungsverfahren zur Herstellung von Essigsäure
DE69313506T3 (de)	2001-11-08	Verfahren zur Herstellung von Essigsäure aus Methanol und Kohlenmonoxyd unter Verwendung eines Rhodiumkatalysators auf einem Träger
DE69502336T2 (de)	1998-09-03	Verfahren zur Herstellung von Essigsäure
DE69608635T3 (de)	2008-11-27	Verfahren zur Herstellung von Essigsäure durch Carbonylierung des Dimethyläthers
EP0071920B1 (fr)	1984-07-11	Procédé de carbonylation d'acétals de la formaldehyde
DE2847241C2 (de)	1984-09-06	Verfahren zur Herstellung von Carbonsäuren oder ihren Estern
DE2741511B2 (de)	1979-09-13	Verfahren zur Herstellung von Butandicarbonsäureestern
DE3037280C2 (de)	1982-10-28	Verfahren zur Herstellung von niedrigmolekularen Monocarbonsäureanhydriden
DD207900A5 (de)	1984-03-21	Verfahren zur karbonylierung von olefinen und organischen estern
DE602004008299T2 (de)	2008-05-08	Verfahren zur carbonylierung von konjugierten dienen mit einem palladium-katalysatorsystem
DE3221172C2 (de)	1984-08-02	Verfahren zur Herstellung von Isobutyrylfluorid
DE68914233T2 (de)	1994-08-18	Verfahren zur Herstellung von Estern von Tricyclodekancarbonsäuren.
DE2820518A1 (de)	1979-11-15	Verfahren zur herstellung von 3- hydroxy-2,2,4-trimethylpentylisobutyrat
DE2823309C2 (fr)	1988-05-11
DE69216856T2 (de)	1997-07-10	Verfahren zur herstellung von adipinsäure
DE2324765C2 (de)	1986-06-26	Verfahren zur Herstellung von Carbonsäureestern
DE2846709C2 (de)	1984-07-12	Verfahren zur Herstellung einer aliphatischen Carbonsäure
DE3729734C2 (fr)	1990-04-12
DE2163031B2 (de)	1976-12-30	Verfahren zur herstellung von terephthalsaeuredimethylester
DE3221174C2 (de)	1985-06-20	Verfahren zur Herstellung von Isobuttersäure
DE3512246C2 (de)	1995-07-20	Verfahren zur Herstellung von Essigsäure
DE69403831T2 (de)	1998-01-02	Verfahren zur Carbonylierung der Allylbutenole und ihrer Ester
DE3249675C2 (de)	1987-01-08	Verfahren zur Herstellung von Methylmethacrylat
DE60303930T2 (de)	2006-10-19	Verfahren zur herstellung von carboxylsäuren
DE1943585A1 (de)	1970-03-05	Verfahren zur Oxydation von Monoarylverbindungen