GB1023423A - Production of adducts of carbon tetrachloride and alkenes - Google Patents
Production of adducts of carbon tetrachloride and alkenesInfo
- Publication number
 - GB1023423A GB1023423A GB34672/61A GB3467262A GB1023423A GB 1023423 A GB1023423 A GB 1023423A GB 34672/61 A GB34672/61 A GB 34672/61A GB 3467262 A GB3467262 A GB 3467262A GB 1023423 A GB1023423 A GB 1023423A
 - Authority
 - GB
 - United Kingdom
 - Prior art keywords
 - carbon tetrachloride
 - reaction
 - adducts
 - tetrachloro
 - catalyst
 - Prior art date
 - Legal status (The legal status 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 status listed.)
 - Expired
 
Links
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 title abstract 19
 - 150000001336 alkenes Chemical class 0.000 title 1
 - 239000000047 product Substances 0.000 abstract 8
 - -1 amine hydrochloride Chemical class 0.000 abstract 6
 - 238000006136 alcoholysis reaction Methods 0.000 abstract 5
 - LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
 - QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 4
 - XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 4
 - ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 abstract 4
 - 239000003054 catalyst Substances 0.000 abstract 4
 - 238000006243 chemical reaction Methods 0.000 abstract 4
 - 229910052801 chlorine Inorganic materials 0.000 abstract 4
 - 125000001309 chloro group Chemical group Cl* 0.000 abstract 4
 - 239000006184 cosolvent Substances 0.000 abstract 4
 - 239000011541 reaction mixture Substances 0.000 abstract 4
 - 150000002430 hydrocarbons Chemical class 0.000 abstract 3
 - TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 abstract 2
 - VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 2
 - KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 abstract 2
 - VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
 - RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
 - BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 2
 - ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
 - 244000028419 Styrax benzoin Species 0.000 abstract 2
 - 235000000126 Styrax benzoin Nutrition 0.000 abstract 2
 - PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
 - 235000008411 Sumatra benzointree Nutrition 0.000 abstract 2
 - 229910021626 Tin(II) chloride Inorganic materials 0.000 abstract 2
 - 150000001299 aldehydes Chemical class 0.000 abstract 2
 - 229910052783 alkali metal Inorganic materials 0.000 abstract 2
 - 125000003545 alkoxy group Chemical group 0.000 abstract 2
 - XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 abstract 2
 - 229960002130 benzoin Drugs 0.000 abstract 2
 - 239000007795 chemical reaction product Substances 0.000 abstract 2
 - 239000003638 chemical reducing agent Substances 0.000 abstract 2
 - 150000001875 compounds Chemical class 0.000 abstract 2
 - 229910052802 copper Inorganic materials 0.000 abstract 2
 - 239000010949 copper Substances 0.000 abstract 2
 - 235000019382 gum benzoic Nutrition 0.000 abstract 2
 - 229910052742 iron Inorganic materials 0.000 abstract 2
 - 238000000034 method Methods 0.000 abstract 2
 - 229920003052 natural elastomer Polymers 0.000 abstract 2
 - 229920001194 natural rubber Polymers 0.000 abstract 2
 - 235000011150 stannous chloride Nutrition 0.000 abstract 2
 - 239000001119 stannous chloride Substances 0.000 abstract 2
 - 229920003051 synthetic elastomer Polymers 0.000 abstract 2
 - 239000005061 synthetic rubber Substances 0.000 abstract 2
 - 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 abstract 2
 - NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
 - VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
 - 239000005977 Ethylene Substances 0.000 abstract 1
 - 125000005042 acyloxymethyl group Chemical group 0.000 abstract 1
 - 125000000217 alkyl group Chemical group 0.000 abstract 1
 - 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
 - 125000003118 aryl group Chemical group 0.000 abstract 1
 - 230000015572 biosynthetic process Effects 0.000 abstract 1
 - 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
 - 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
 - 229920001971 elastomer Polymers 0.000 abstract 1
 - 229910052736 halogen Inorganic materials 0.000 abstract 1
 - 150000002367 halogens Chemical group 0.000 abstract 1
 - 229930195733 hydrocarbon Natural products 0.000 abstract 1
 - 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
 - 229920000126 latex Polymers 0.000 abstract 1
 - TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 abstract 1
 - 150000002825 nitriles Chemical group 0.000 abstract 1
 - 239000001294 propane Substances 0.000 abstract 1
 - 239000005060 rubber Substances 0.000 abstract 1
 - 238000003786 synthesis reaction Methods 0.000 abstract 1
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
 - C08C19/00—Chemical modification of rubber
 - C08C19/12—Incorporating halogen atoms into the molecule
 - C08C19/18—Incorporating halogen atoms into the molecule by reaction with hydrocarbons substituted by halogen
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C17/00—Preparation of halogenated hydrocarbons
 - C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
 - C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
 - C07C17/275—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of hydrocarbons and halogenated hydrocarbons
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C17/00—Preparation of halogenated hydrocarbons
 - C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
 - C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
 - C07C17/278—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of only halogenated hydrocarbons
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C19/00—Acyclic saturated compounds containing halogen atoms
 - C07C19/01—Acyclic saturated compounds containing halogen atoms containing chlorine
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C21/00—Acyclic unsaturated compounds containing halogen atoms
 - C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
 - C07C21/04—Chloro-alkenes
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C22/00—Cyclic compounds containing halogen atoms bound to an acyclic carbon atom
 - C07C22/02—Cyclic compounds containing halogen atoms bound to an acyclic carbon atom having unsaturation in the rings
 - C07C22/04—Cyclic compounds containing halogen atoms bound to an acyclic carbon atom having unsaturation in the rings containing six-membered aromatic rings
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C43/00—Ethers; Compounds having groups, groups or groups
 - C07C43/02—Ethers
 - C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
 - C07C43/14—Unsaturated ethers
 - C07C43/17—Unsaturated ethers containing halogen
 - C07C43/174—Unsaturated ethers containing halogen containing six-membered aromatic rings
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
 - C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
 - C07C51/363—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
 - C07C53/15—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing halogen
 - C07C53/19—Acids containing three or more carbon atoms
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Chemical Kinetics & Catalysis (AREA)
 - General Chemical & Material Sciences (AREA)
 - Health & Medical Sciences (AREA)
 - Medicinal Chemistry (AREA)
 - Polymers & Plastics (AREA)
 - Engineering & Computer Science (AREA)
 - Oil, Petroleum & Natural Gas (AREA)
 - Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
 - Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
 
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| IL1607961 | 1961-09-28 | ||
| IL1608061 | 1961-09-28 | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| GB1023423A true GB1023423A (en) | 1966-03-23 | 
Family
ID=26320401
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| GB34672/61A Expired GB1023423A (en) | 1961-09-28 | 1962-09-11 | Production of adducts of carbon tetrachloride and alkenes | 
| GB34673/62A Expired GB1022684A (en) | 1961-09-28 | 1962-09-11 | Adducts of alkenes with chloroform and methods of producing them | 
| GB12585/66A Expired GB1146463A (en) | 1961-09-28 | 1966-03-22 | Production of adducts of carbon tetrachloride and olefinic compounds | 
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| GB34673/62A Expired GB1022684A (en) | 1961-09-28 | 1962-09-11 | Adducts of alkenes with chloroform and methods of producing them | 
| GB12585/66A Expired GB1146463A (en) | 1961-09-28 | 1966-03-22 | Production of adducts of carbon tetrachloride and olefinic compounds | 
Country Status (5)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US4271325A (en) * | 1976-11-18 | 1981-06-02 | Stauffer Chemical Company | Process for the manufacture of 1,1-dihalo-4-methyl-1,3-pentadienes | 
| CN111902384A (zh) * | 2018-04-03 | 2020-11-06 | 蓝立方知识产权有限责任公司 | 在氯化烷烃生产中回收催化剂的方法 | 
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US3399241A (en) * | 1964-02-26 | 1968-08-27 | Olin Mathieson | Process for preparing 2, 4, 4, 4-tetrachlorobutanol from allyl alcohol and ccl4 in the presence of powdered iron catalyst | 
| US3399217A (en) * | 1964-03-04 | 1968-08-27 | Olin Mathieson | Catalyst system for reaction of an allyl alcohol and carbon tetrachloride to produce2, 4, 4, 4-tetrachlorobutanol | 
| US3993586A (en) * | 1973-04-11 | 1976-11-23 | Bayer Aktiengesellschaft | Water-soluble complex of cuprous chloride, hydrochloric acid and at least one amine or amine salt | 
| GB1498931A (en) * | 1975-02-12 | 1978-01-25 | Sumitomo Chemical Co | Tetrahalopentyl ketone derivatives processes for producing them and their conversion to beta-dihaloethenylcyclopropane derivatives | 
| JPS5259103A (en) * | 1975-11-10 | 1977-05-16 | Shin Etsu Chem Co Ltd | Process for preparation of tetrachloroalkane | 
| US4036897A (en) * | 1976-08-04 | 1977-07-19 | The Lummus Company | Production of hexachlorocyclopentadiene | 
| FR2425451A1 (fr) * | 1978-05-09 | 1979-12-07 | Anvar | Procede pour l'addition de groupes trihalogenomethyle fonctionnels sur des polyalcadienes | 
| DE3111848A1 (de) * | 1981-03-26 | 1982-10-14 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von substituierten (alpha)-halogen-propionsaeuren und ihren derivaten | 
| DE3136983A1 (de) * | 1981-09-17 | 1983-03-31 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von 1,1,1-trichlormethylverbindungen | 
| US4691065A (en) * | 1983-11-02 | 1987-09-01 | Occidental Chemical Corporation | Chlorotrifluoroethylene telomerization process | 
| BE1005095A3 (fr) * | 1991-07-10 | 1993-04-20 | Solvay | Procede pour la preparation de 1,1-dichloro-1,3,3,3-tetrafluoropropane. | 
| US5395997A (en) * | 1993-07-29 | 1995-03-07 | Alliedsignal Inc. | Process for the preparation of hydrofluorocarbons having 3 to 7 carbon atoms | 
| CA2166971C (en) * | 1993-07-29 | 2005-09-27 | Michael Van Der Puy | Process for the preparation of 1,1,1,3,3-pentafluoropropane | 
| WO1996001797A1 (en) * | 1994-07-11 | 1996-01-25 | Alliedsignal Inc. | Process for the manufacture of 1,1,1,3,3-pentafluoropropane | 
| US6291730B1 (en) | 1995-08-01 | 2001-09-18 | E. I. Du Pont De Nemours And Company | Process for the manufacture of halocarbons and selected compounds and azeotropes with HF | 
| US6755942B1 (en) * | 1995-08-01 | 2004-06-29 | E. I. Du Pont De Nemours And Company | Process for the manufacture of halocarbons and selected compounds and azeotropes with HF | 
| US5633413A (en) * | 1995-08-08 | 1997-05-27 | Alliedsignal Inc. | Continuous process for the production of vinylidene chloride telomers | 
| US5817893A (en) * | 1996-06-18 | 1998-10-06 | E. I. Du Pont De Nemours And Company | Processes for the manufacture and purification of 1,1,2,2,3,3,4,4-octafluorobutane and by-products | 
| JP2001508462A (ja) * | 1997-01-16 | 2001-06-26 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | ハロカーボンの製造方法 | 
| CN1131849C (zh) | 1997-05-05 | 2003-12-24 | 索尔维公司 | 制备1,1,1,3,3-五氯丁烷的方法 | 
| ES2218829T3 (es) * | 1997-05-05 | 2004-11-16 | Solvay (Societe Anonyme) | Procedimiento de preparacion de hidrocarburos halogenados. | 
| BE1011319A3 (fr) * | 1997-05-05 | 1999-07-06 | Solvay | Procede de preparation d'hydrocarbures halogenes. | 
| BE1011249A3 (fr) * | 1997-07-03 | 1999-06-01 | Solvay | Pentachlorobutane, son procede de fabrication et son utilisation, procede de preparation du 1,1-difluoro-2-trifluoromethylpropane et utilisation de ce compose. | 
| DE69810301T2 (de) | 1997-08-08 | 2003-10-02 | Solvay S.A., Bruessel/Bruxelles | Verfahren zur herstellung von halogenierten kohlenwasserstoffen | 
| US6187976B1 (en) | 1998-04-09 | 2001-02-13 | Alliedsignal Inc. | Process for the preparation of fluorine containing hydrohalocarbons | 
| BE1012268A3 (fr) | 1998-11-05 | 2000-08-01 | Solvay | Procede de preparation d'hydrocarbures halogenes. | 
| US7253047B2 (en) * | 1999-09-01 | 2007-08-07 | Micron Technology, Inc. | Semiconductor processing methods of forming transistors, semiconductor processing methods of forming dynamic random access memory circuitry, and related integrated circuitry | 
| ES2320850T5 (es) | 1999-10-06 | 2012-07-03 | Solvay (Société Anonyme) | Procedimiento de preparación de hidrocarburos halogenados en presencia de un cocatalizador | 
| ATE267790T1 (de) | 1999-10-06 | 2004-06-15 | Solvay | Verfahren zur herstellung von halogenierten kohlenwasserstoffen | 
| CN100386691C (zh) * | 2002-06-21 | 2008-05-07 | 洛斯阿拉莫斯国家安全股份有限公司 | 含有离子液体的电光装置、电光汽车镜及其所用的电解液 | 
| US20040225166A1 (en) * | 2003-05-05 | 2004-11-11 | Vulcan Chemicals A Business Group Of Vulcan Materials Company | Method for producing 1,1,1,3-tetrachloropropane and other haloalkanes with iron catalyst | 
| US20050049443A1 (en) * | 2003-08-28 | 2005-03-03 | Vulcan Chemicals A Business Group Of Vulcan Materials Company | Method for producing 1,1,1,3-tetrachloropropane and other haloalkanes using a copper catalyst | 
| CN101522597B (zh) | 2006-10-03 | 2013-05-29 | 墨西哥化学阿玛科股份有限公司 | 通过脱卤化氢制备c3-c6(氢)氟烯烃的方法 | 
| US9738577B2 (en) * | 2006-10-11 | 2017-08-22 | Honeywell International Inc. | Process for the manufacture of 1,1,1,3,3-pentachloropropane | 
| CA2739924C (en) * | 2008-10-13 | 2017-03-07 | Dow Global Technologies Llc | Process for the production of chlorinated and/or fluorinated propenes | 
| 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) | 
| 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 | 
| US8581011B2 (en) * | 2009-10-09 | 2013-11-12 | Dow Global Technologies, Llc | Process for the production of chlorinated and/or fluorinated propenes | 
| US20110087056A1 (en) * | 2009-10-09 | 2011-04-14 | Dow Global Technologies | Adiabatic plug flow reactors and processes incorporating the same | 
| US8426655B2 (en) | 2010-03-26 | 2013-04-23 | Honeywell International Inc. | Process for the manufacture of hexafluoro-2-butene | 
| 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 | 
| EP2714630A1 (en) | 2011-05-31 | 2014-04-09 | Dow Global Technologies LLC | Process for the production of chlorinated propenes | 
| 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 | 
| US9199899B2 (en) | 2011-12-02 | 2015-12-01 | Blue Cube Ip 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 | 
| 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 | 
| CN104230751B (zh) * | 2014-06-16 | 2016-05-25 | 浙江中欣氟材股份有限公司 | 一种2,4,4,4-四氯丁腈的合成方法 | 
| CN104230752B (zh) * | 2014-08-22 | 2016-05-25 | 浙江中欣氟材股份有限公司 | 一种2,4,4,4-四氯丁腈的制备方法 | 
- 
        0
        
- BE BE622939D patent/BE622939A/xx unknown
 - BE BE622938D patent/BE622938A/xx unknown
 
 - 
        1962
        
- 1962-09-11 GB GB34672/61A patent/GB1023423A/en not_active Expired
 - 1962-09-11 GB GB34673/62A patent/GB1022684A/en not_active Expired
 - 1962-09-26 DE DEP1268605A patent/DE1268605B/de active Pending
 - 1962-09-26 DE DEP1269618A patent/DE1269618B/de active Pending
 - 1962-09-27 FR FR910638A patent/FR1335343A/fr not_active Expired
 - 1962-09-27 FR FR910636A patent/FR1334749A/fr not_active Expired
 
 - 
        1965
        
- 1965-07-27 US US475274A patent/US3651019A/en not_active Expired - Lifetime
 
 - 
        1966
        
- 1966-03-22 GB GB12585/66A patent/GB1146463A/en not_active Expired
 
 
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US4271325A (en) * | 1976-11-18 | 1981-06-02 | Stauffer Chemical Company | Process for the manufacture of 1,1-dihalo-4-methyl-1,3-pentadienes | 
| CN111902384A (zh) * | 2018-04-03 | 2020-11-06 | 蓝立方知识产权有限责任公司 | 在氯化烷烃生产中回收催化剂的方法 | 
| CN111902384B (zh) * | 2018-04-03 | 2024-05-14 | 蓝立方知识产权有限责任公司 | 在氯化烷烃生产中回收催化剂的方法 | 
Also Published As
| Publication number | Publication date | 
|---|---|
| DE1269618B (de) | 1968-06-06 | 
| FR1335343A (fr) | 1963-08-16 | 
| GB1146463A (en) | 1969-03-26 | 
| DE1268605B (de) | 1968-05-22 | 
| BE622939A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| GB1022684A (en) | 1966-03-16 | 
| US3651019A (en) | 1972-03-21 | 
| BE622938A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| FR1334749A (fr) | 1963-08-09 | 
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