CH473072A - Procédé pour la préparation de dioléfines - Google Patents

Procédé pour la préparation de dioléfines

Info

Publication number: CH473072A
Authority: CH; Switzerland
Prior art keywords: sep; halide; sub; diolefins; temperature
Prior art date: 1966-06-07

Application number

CH1544866A

Other languages

English (en)

French (fr)

Inventor

Bell Hayes William

Original Assignee

El Paso Products Co

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.)

1966-06-07

Filing date

1966-10-25

Publication date

1969-05-31

1966-10-25 Application filed by El Paso Products Co filed Critical El Paso Products Co

1969-05-31 Publication of CH473072A publication Critical patent/CH473072A/fr

Links

238000000034 method Methods 0.000 title claims description 20
150000001993 dienes Chemical class 0.000 title claims description 13
238000002360 preparation method Methods 0.000 title claims description 6
238000006243 chemical reaction Methods 0.000 claims description 16
150000004820 halides Chemical class 0.000 claims description 14
150000001336 alkenes Chemical class 0.000 claims description 10
-1 allylic halide Chemical class 0.000 claims description 10
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 9
OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical group ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 claims description 8
239000003153 chemical reaction reagent Substances 0.000 claims description 6
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 6
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 6
238000009833 condensation Methods 0.000 claims description 5
230000005494 condensation Effects 0.000 claims description 5
125000005843 halogen group Chemical group 0.000 claims description 3
125000002877 alkyl aryl group Chemical group 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
239000007858 starting material Substances 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
150000001875 compounds Chemical class 0.000 description 4
239000000543 intermediate Substances 0.000 description 4
239000000203 mixture Substances 0.000 description 4
238000000197 pyrolysis Methods 0.000 description 4
230000035484 reaction time Effects 0.000 description 4
230000009466 transformation Effects 0.000 description 4
239000007789 gas Substances 0.000 description 3
PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
125000000746 allylic group Chemical group 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
230000008034 disappearance Effects 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
DMAYBPBPEUFIHJ-UHFFFAOYSA-N 4-bromobut-1-ene Chemical compound BrCCC=C DMAYBPBPEUFIHJ-UHFFFAOYSA-N 0.000 description 1
WKEVRZCQFQDCIR-UHFFFAOYSA-N 4-chlorobut-1-ene Chemical compound ClCCC=C WKEVRZCQFQDCIR-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
239000004677 Nylon Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
150000001348 alkyl chlorides Chemical class 0.000 description 1
238000005915 ammonolysis reaction Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000005755 formation reaction Methods 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
239000012433 hydrogen halide Substances 0.000 description 1
229910000039 hydrogen halide Inorganic materials 0.000 description 1
238000005647 hydrohalogenation reaction Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000011084 recovery Methods 0.000 description 1
238000004064 recycling Methods 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
229910052709 silver Inorganic materials 0.000 description 1
239000004332 silver Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/86—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon
- C07C2/861—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only halogen as hetero-atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH1544866A 1966-06-07 1966-10-25 Procédé pour la préparation de dioléfines CH473072A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US55567166A	1966-06-07	1966-06-07

Publications (1)

Publication Number	Publication Date
CH473072A true CH473072A (fr)	1969-05-31

Family

ID=24218178

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1544866A CH473072A (fr)	1966-06-07	1966-10-25	Procédé pour la préparation de dioléfines

Country Status (6)

Country	Link
AT (1)	AT263734B (de)
BE (1)	BE688911A (de)
CH (1)	CH473072A (de)
ES (1)	ES332724A1 (de)
LU (1)	LU52247A1 (de)
NL (1)	NL6615826A (de)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR112012007916A2 (pt)	2009-10-09	2019-09-24	Dow Global Technologies Llc	processo de etapa para a produção de propenos clorados ou fluorados e processo para preparar 1,1,3,3 - tetrafluorprop-1-eno
JP5767231B2 (ja)	2009-10-09	2015-08-19	ダウグローバルテクノロジーズエルエルシー	塩素化及び／又はフッ素化されたプロペン及びより高級なアルケンを製造するプロセス
JP5782038B2 (ja)	2009-10-09	2015-09-24	ダウグローバルテクノロジーズエルエルシー	等温多管式反応器及び該反応器を組み込んだプロセス
WO2012166394A1 (en)	2011-05-31	2012-12-06	Dow Global Technologies, Llc	Process for the production of chlorinated propenes
JP6212035B2 (ja)	2011-05-31	2017-10-11	ブルーキューブアイピーエルエルシー	塩素化プロペンの製造方法
JP6267114B2 (ja)	2011-06-08	2018-01-24	ダウアグロサイエンシィズエルエルシー	塩素化および／またはフッ素化プロペンを生成するためのプロセス
CN103717557A (zh)	2011-08-07	2014-04-09	陶氏环球技术有限责任公司	生产氯化的丙烯的方法
CN108929192A (zh)	2011-08-07	2018-12-04	蓝立方知识产权有限责任公司	生产氯化的丙烯的方法
IN2014CN03748A (de)	2011-11-21	2015-09-25	Dow Global Technologies Llc
CA2856545A1 (en)	2011-12-02	2013-06-06	Dow Global Technologies Llc	Process for the production of chlorinated alkanes
JP6050375B2 (ja)	2011-12-02	2016-12-21	ブルーキューブアイピーエルエルシー	クロロアルカンの製造方法
JP6170068B2 (ja)	2011-12-13	2017-07-26	ブルーキューブアイピーエルエルシー	塩素化プロパン及びプロペンの製造方法
IN2014CN04418A (de)	2011-12-22	2015-09-04	Dow Global Technologies Llc
WO2013096706A1 (en) *	2011-12-23	2013-06-27	Dow Global Technologies, Llc	Process for the production of alkenes and/or aromatic compounds
US9598334B2 (en)	2012-09-20	2017-03-21	Blue Cube Ip Llc	Process for the production of chlorinated propenes
EP2897930A1 (de)	2012-09-20	2015-07-29	Dow Global Technologies LLC	Verfahren zur herstellung von chlorierten propenen
CA2885329A1 (en)	2012-09-30	2014-03-04	Dow Global Technologies Llc	Weir quench and processes incorporating the same
US10065157B2 (en)	2012-10-26	2018-09-04	Blue Cube Ip Llc	Mixer and processes incorporating the same
JP6247311B2 (ja)	2012-12-18	2017-12-13	ブルーキューブアイピーエルエルシー	塩素化プロペンを生成するための方法
CA2894168C (en)	2012-12-19	2018-04-24	Dow Global Technologies Llc	Process for the production of chlorinated propenes
CA2901450A1 (en)	2013-02-27	2014-09-04	Blue Cube Ip Llc	Process for the production of chlorinated propenes
CA2903760C (en)	2013-03-09	2018-02-20	Blue Cube Ip Llc	Process for the production of chlorinated alkanes

1966
- 1966-10-25 ES ES0332724A patent/ES332724A1/es not_active Expired
- 1966-10-25 AT AT995566A patent/AT263734B/de active
- 1966-10-25 CH CH1544866A patent/CH473072A/fr not_active IP Right Cessation
- 1966-10-26 LU LU52247D patent/LU52247A1/xx unknown
- 1966-10-26 BE BE688911D patent/BE688911A/xx unknown
- 1966-11-09 NL NL6615826A patent/NL6615826A/xx unknown

Also Published As

Publication number	Publication date
AT263734B (de)	1968-08-12
LU52247A1 (de)	1966-12-28
BE688911A (de)	1967-04-26
ES332724A1 (es)	1967-12-01
NL6615826A (de)	1967-12-08

Legal Events

Date	Code	Title	Description
1978-05-31	PL	Patent ceased

Publication	Publication Date	Title
CH473072A (fr)	1969-05-31	Procédé pour la préparation de dioléfines
EP0173390B1 (de)	1989-02-01	Verfahren zur substitutiven Chlorierung von organischen Verbindungen mit molekulärem Chlor in Gegenwart eines Chlorierungsproduktes als Initiator sowie die Verwendung solcher Initiator
FR2744442A1 (fr)	1997-08-08	Preparation du 1,1,1,3,3-pentachlorobutane et du 1,1,1,3,3,-pentafluorobutane
HUP9901285A2 (hu)	1999-07-28	Eljárás difluor-metán előállítására
JPS60237030A (ja)	1985-11-25	１，２，３‐トリクロル‐２‐メチループロンの製法
NO174586B (no)	1994-02-21	Syntese av karbonylforbindelser
US4824987A (en)	1989-04-25	Method of preparing m-trifluoromethylphenyl acetonitrile
US2509160A (en)	1950-05-23	Making hexachlorocyclopentadiene
CA1305726C (fr)	1992-07-28	Procede de preparation du citral
EP0172595B1 (de)	1989-01-25	Verfahren zur Herstellung von chlorierten Pyridinderivaten und radikal Initiatoren verwendet in diesem Verfahren
UA78613C2 (en)	2007-04-10	A process for the production of 3-methylthiopropanal and a process for the production of 2-hydroxy-4-(methylthio)butanenitrile
JP2006515834A5 (de)	2010-04-22
He et al.	1999	The photochemical synthesis of α, α, α-bromodifluorotoluene and α, α, α-chlorodifluorotoluene
RU2144019C1 (ru)	2000-01-10	Способ получения пентафторйодэтана
US3739007A (en)	1973-06-12	Process for preparing aliphatic nitriles of increased carbon chain length
US3414622A (en)	1968-12-03	Production of hexamethylenediamine
US3379764A (en)	1968-04-23	Amination of alkylbromides
EP0357103B1 (de)	1992-09-30	Verfahren zur Herstellung von 2,6-Dichlorpyridin und die Verwendung von bis(Trichloromethyl)sulphon dafür
US2490386A (en)	1949-12-06	Production of unsaturated acid halides
GB2142018A (en)	1985-01-09	Method for producing 2,6-difluorobenzonitrile
US3855264A (en)	1974-12-17	Preparation of halogenated benzonitrile
RU2129114C1 (ru)	1999-04-20	Способ получения третичного бутилхлорида
EP0004804B1 (de)	1980-10-29	Verfahren zur Dimerisierung von Olefinen mit 8-20 Kohlenstoffatomen und dadurch erhaltene Dimere von Olefinen
EP0140438B1 (de)	1989-09-06	Verfahren zur Herstellung von 2-Chloropyridin
SU372215A1 (ru)	1973-03-01	ВСШОЮЗНАЯ IПЯ^?'?4ТНГ1.; •• ViJ^^rr vftj-jl