CH473072A - Procédé pour la préparation de dioléfines - Google Patents
Procédé pour la préparation de dioléfinesInfo
- Publication number
- CH473072A CH473072A CH1544866A CH1544866A CH473072A CH 473072 A CH473072 A CH 473072A CH 1544866 A CH1544866 A CH 1544866A CH 1544866 A CH1544866 A CH 1544866A CH 473072 A CH473072 A CH 473072A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- halide
- sub
- diolefins
- temperature
- Prior art date
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)
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 (instruction) |
| BE (1) | BE688911A (instruction) |
| CH (1) | CH473072A (instruction) |
| ES (1) | ES332724A1 (instruction) |
| LU (1) | LU52247A1 (instruction) |
| NL (1) | NL6615826A (instruction) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8581011B2 (en) | 2009-10-09 | 2013-11-12 | Dow Global Technologies, Llc | Process for the production of chlorinated and/or fluorinated propenes |
| US8581012B2 (en) | 2009-10-09 | 2013-11-12 | Dow Global Technologies, Llc | Processes for the production of chlorinated and/or fluorinated propenes and higher alkenes |
| BR112012007914A2 (pt) | 2009-10-09 | 2019-09-24 | Dow Global Technologies Llc | reator isotérmico de tubos múltiplos, processo para produzir um propeno clorado ou fluorado e processo para preparar 2,3,3,3- tetrafluorprop-1-eno (hfo-1234yf) ou 1,3,3,3- tetrafluorprop-1-eno (hfo-1234ze) |
| EP2714630A1 (en) | 2011-05-31 | 2014-04-09 | Dow Global Technologies LLC | Process for the production of chlorinated propenes |
| JP5918358B2 (ja) | 2011-05-31 | 2016-05-18 | 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 |
| CN103596908A (zh) | 2011-06-08 | 2014-02-19 | 陶氏益农公司 | 生产氯化和/或氟化丙烯的方法 |
| US9233896B2 (en) | 2011-08-07 | 2016-01-12 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
| 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 |
| WO2013078035A1 (en) | 2011-11-21 | 2013-05-30 | Dow Global Technologies, Llc | Process for the production of chlorinated alkanes |
| US9284239B2 (en) | 2011-12-02 | 2016-03-15 | Blue Cube Ip Llc | Process for the production of chlorinated alkanes |
| US9199899B2 (en) | 2011-12-02 | 2015-12-01 | Blue Cube Ip Llc | Process for the production of chlorinated alkanes |
| 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 |
| JP2015503523A (ja) | 2011-12-22 | 2015-02-02 | ダウ グローバル テクノロジーズ エルエルシー | テトラクロロメタンの製造方法 |
| BR112014015123A2 (pt) * | 2011-12-23 | 2017-06-13 | Dow Global Technologies Llc | processo para a produção de um ou mais alcenos ou compostos aromáticos |
| EP2897930A1 (en) | 2012-09-20 | 2015-07-29 | Dow Global Technologies LLC | Process for the production of chlorinated propenes |
| WO2014046977A1 (en) | 2012-09-20 | 2014-03-27 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
| CN104718020A (zh) | 2012-09-30 | 2015-06-17 | 陶氏环球技术有限公司 | 堰式骤冷器和并入所述堰式骤冷器的工艺 |
| CA2887559A1 (en) | 2012-10-26 | 2014-05-01 | Dow Global Technologies Llc | Mixer and reactor and process 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 |
| US9475740B2 (en) | 2012-12-19 | 2016-10-25 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
| WO2014134233A2 (en) | 2013-02-27 | 2014-09-04 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
| CN105026348A (zh) | 2013-03-09 | 2015-11-04 | 蓝立方知识产权有限责任公司 | 用于生产氯化烷烃的方法 |
-
1966
- 1966-10-25 CH CH1544866A patent/CH473072A/fr not_active IP Right Cessation
- 1966-10-25 AT AT995566A patent/AT263734B/de active
- 1966-10-25 ES ES0332724A patent/ES332724A1/es not_active Expired
- 1966-10-26 BE BE688911D patent/BE688911A/xx unknown
- 1966-10-26 LU LU52247D patent/LU52247A1/xx unknown
- 1966-11-09 NL NL6615826A patent/NL6615826A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AT263734B (de) | 1968-08-12 |
| ES332724A1 (es) | 1967-12-01 |
| LU52247A1 (instruction) | 1966-12-28 |
| BE688911A (instruction) | 1967-04-26 |
| NL6615826A (instruction) | 1967-12-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |