IL41101A - Process for preparing 1,2,3-trichloropropene - Google Patents

Process for preparing 1,2,3-trichloropropene

Info

Publication number: IL41101A
Authority: IL; Israel
Prior art keywords: catalyst; temperature; tetrachloropropane; reaction; oxides
Prior art date: 1971-12-17

Application number

IL41101A

Other languages

English (en)

Other versions

IL41101A0 (en

Original Assignee

Monsanto 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.)

1971-12-17

Filing date

1972-12-15

Publication date

1977-05-31

1971-12-27 Priority claimed from US00212742A external-priority patent/US3823195A/en

1972-12-15 Application filed by Monsanto Co filed Critical Monsanto Co

1973-02-28 Publication of IL41101A0 publication Critical patent/IL41101A0/xx

1977-05-31 Publication of IL41101A publication Critical patent/IL41101A/en

Links

238000004519 manufacturing process Methods 0.000 title description 6
HIILBTHBHCLUER-IWQZZHSRSA-N (z)-1,2,3-trichloroprop-1-ene Chemical compound ClC\C(Cl)=C\Cl HIILBTHBHCLUER-IWQZZHSRSA-N 0.000 title 1
239000003054 catalyst Substances 0.000 claims description 44
238000000034 method Methods 0.000 claims description 41
238000006243 chemical reaction Methods 0.000 claims description 17
FEKGWIHDBVDVSM-UHFFFAOYSA-N 1,1,1,2-tetrachloropropane Chemical compound CC(Cl)C(Cl)(Cl)Cl FEKGWIHDBVDVSM-UHFFFAOYSA-N 0.000 claims description 11
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 8
229960000892 attapulgite Drugs 0.000 claims description 7
229910052625 palygorskite Inorganic materials 0.000 claims description 7
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
229910052782 aluminium Inorganic materials 0.000 claims description 4
239000011777 magnesium Substances 0.000 claims description 4
229910052749 magnesium Inorganic materials 0.000 claims description 4
239000001294 propane Substances 0.000 claims description 4
239000012808 vapor phase Substances 0.000 claims description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
238000007033 dehydrochlorination reaction Methods 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
239000003518 caustics Substances 0.000 description 7
LIPPKMMVZOHCIF-UHFFFAOYSA-N 1,1,2-trichloroprop-1-ene Chemical compound CC(Cl)=C(Cl)Cl LIPPKMMVZOHCIF-UHFFFAOYSA-N 0.000 description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
239000000460 chlorine Substances 0.000 description 6
229910052801 chlorine Inorganic materials 0.000 description 6
239000000463 material Substances 0.000 description 6
239000000203 mixture Substances 0.000 description 6
239000000047 product Substances 0.000 description 6
238000005660 chlorination reaction Methods 0.000 description 5
239000004927 clay Substances 0.000 description 5
239000008187 granular material Substances 0.000 description 5
239000007788 liquid Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
239000011521 glass Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
230000007420 reactivation Effects 0.000 description 4
238000004821 distillation Methods 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 3
239000000391 magnesium silicate Substances 0.000 description 3
229910052919 magnesium silicate Inorganic materials 0.000 description 3
235000019792 magnesium silicate Nutrition 0.000 description 3
229910052624 sepiolite Inorganic materials 0.000 description 3
235000019355 sepiolite Nutrition 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000004215 Carbon black (E152) Substances 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
239000004113 Sepiolite Substances 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical class O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 description 2
230000003197 catalytic effect Effects 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000007789 gas Substances 0.000 description 2
230000002363 herbicidal effect Effects 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
229910052500 inorganic mineral Chemical class 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
238000006317 isomerization reaction Methods 0.000 description 2
239000011707 mineral Chemical class 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
238000012856 packing Methods 0.000 description 2
239000002245 particle Substances 0.000 description 2
239000011148 porous material Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
-1 silicon aluminum magnesium Chemical compound 0.000 description 2
239000002699 waste material Substances 0.000 description 2
OWXJKYNZGFSVRC-NSCUHMNNSA-N (e)-1-chloroprop-1-ene Chemical compound C\C=C\Cl OWXJKYNZGFSVRC-NSCUHMNNSA-N 0.000 description 1
SBMYBOVJMOVVQW-UHFFFAOYSA-N 2-[3-[[4-(2,2-difluoroethyl)piperazin-1-yl]methyl]-4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound FC(CN1CCN(CC1)CC1=NN(C=C1C=1C=NC(=NC=1)NC1CC2=CC=CC=C2C1)CC(=O)N1CC2=C(CC1)NN=N2)F SBMYBOVJMOVVQW-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000283986 Lepus Species 0.000 description 1
229910000792 Monel Inorganic materials 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
YXOXBCQDQJEUTB-UHFFFAOYSA-N [3,4-di(propan-2-yl)thiophen-2-yl]carbamic acid Chemical compound CC(C)C1=CSC(NC(O)=O)=C1C(C)C YXOXBCQDQJEUTB-UHFFFAOYSA-N 0.000 description 1
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
CNLWCVNCHLKFHK-UHFFFAOYSA-N aluminum;lithium;dioxido(oxo)silane Chemical compound [Li+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O CNLWCVNCHLKFHK-UHFFFAOYSA-N 0.000 description 1
239000011324 bead Substances 0.000 description 1
229910052790 beryllium Inorganic materials 0.000 description 1
ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003575 carbonaceous material Substances 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
230000009849 deactivation Effects 0.000 description 1
238000006704 dehydrohalogenation reaction Methods 0.000 description 1
238000003795 desorption Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000005826 halohydrocarbons Chemical class 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
QRNPTSGPQSOPQK-UHFFFAOYSA-N magnesium zirconium Chemical compound [Mg].[Zr] QRNPTSGPQSOPQK-UHFFFAOYSA-N 0.000 description 1
230000001473 noxious effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000002243 precursor Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
229910052642 spodumene Inorganic materials 0.000 description 1
239000007858 starting material Substances 0.000 description 1
230000008016 vaporization Effects 0.000 description 1
239000006200 vaporizer Substances 0.000 description 1
239000011800 void material Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
- C07C17/04—Preparation of halogenated hydrocarbons by addition of halogens to unsaturated halogenated hydrocarbons
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
- C07C17/358—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by isomerisation
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C21/00—Acyclic unsaturated compounds containing halogen atoms
- 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

Landscapes

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

IL41101A 1971-12-17 1972-12-15 Process for preparing 1,2,3-trichloropropene IL41101A (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US21026871A	1971-12-17	1971-12-17
US00212742A US3823195A (en)	1971-12-27	1971-12-27	Preparation of 1,1,2,3-tetrachloropropene from 1,2,3-trichloropropane
US30216372A	1972-10-30	1972-10-30

Publications (2)

Publication Number	Publication Date
IL41101A0 IL41101A0 (en)	1973-02-28
IL41101A true IL41101A (en)	1977-05-31

Family

ID=27395474

Family Applications (3)

Application Number	Title	Priority Date	Filing Date
IL41101A IL41101A (en)	1971-12-17	1972-12-15	Process for preparing 1,2,3-trichloropropene
IL50070A IL50070A (en)	1971-12-17	1972-12-15	Process for the production of 1,1,2,3-tetrachloropropene
IL7650070A IL50070A0 (en)	1971-12-17	1976-07-20	Process for the production of 1,1,2,3-tetrachloropropene

Family Applications After (2)

Application Number	Title	Priority Date	Filing Date
IL50070A IL50070A (en)	1971-12-17	1972-12-15	Process for the production of 1,1,2,3-tetrachloropropene
IL7650070A IL50070A0 (en)	1971-12-17	1976-07-20	Process for the production of 1,1,2,3-tetrachloropropene

Country Status (13)

Country	Link
JP (2)	JPS4867209A (2)
BE (1)	BE792789A (2)
BG (1)	BG21599A3 (2)
CH (1)	CH584173A5 (2)
DD (1)	DD101140A5 (2)
DE (1)	DE2261516C3 (2)
FR (2)	FR2169817B1 (2)
GB (1)	GB1381619A (2)
IL (3)	IL41101A (2)
IT (1)	IT974728B (2)
NL (1)	NL160542C (2)
RO (1)	RO60573A (2)
YU (1)	YU39903B (2)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SI3336074T1 (sl) *	2006-01-03	2025-09-30	Honeywell International Inc.	Postopek za proizvodnjo fluoriranih organskih spojin
US8258355B2 (en) *	2007-07-25	2012-09-04	Honeywell International Inc.	Processes for preparing 1,1,2,3-tetrachloropropene
DK2231565T3 (da)	2007-12-19	2014-05-26	Occidental Chem Co	Fremgangsmåder til fremstilling af clorerede carbonhydrider
CN102177116B (zh)	2009-06-24	2014-07-16	株式会社德山	氯化烃的制备方法
EP2485996B1 (en)	2009-10-09	2016-06-15	Blue Cube IP LLC	Process for the production of chlorinated and/or fluorinated propenes
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
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
CN103562164B (zh)	2011-05-31	2016-04-20	陶氏环球技术有限责任公司	生产氯化丙烯类的方法
US9056808B2 (en)	2011-05-31	2015-06-16	Dow Global Technologies, Llc	Process for the production of chlorinated propenes
KR102007722B1 (ko)	2011-06-08	2019-08-07	다우 글로벌 테크놀로지스 엘엘씨	염화 및/또는 불화 프로펜의 제조 방법
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
US8907148B2 (en)	2011-08-07	2014-12-09	Dow Global Technologies Llc	Process for the production of chlorinated propenes
WO2013074394A1 (en) *	2011-11-18	2013-05-23	Dow Global Technologies, Llc	Process for the production of chlorinated propanes and/or propenes
IN2014CN03748A (2)	2011-11-21	2015-09-25	Dow Global Technologies Llc
JP6059246B2 (ja)	2011-12-02	2017-01-11	ブルーキューブアイピーエルエルシー	塩素化アルカンの製造方法
EP2785671B1 (en)	2011-12-02	2017-03-01	Blue Cube IP LLC	Process for the production of chlorinated propanes
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
CN104011000A (zh)	2011-12-22	2014-08-27	陶氏环球技术有限责任公司	生产四氯甲烷的方法
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
EP2897932A1 (en)	2012-09-20	2015-07-29	Dow Global Technologies LLC	Process for the production of chlorinated propenes
JP6272878B2 (ja)	2012-09-30	2018-01-31	ブルーキューブアイピーエルエルシー	せきクエンチおよびそれを組み込んだ方法
EP2911773B1 (en)	2012-10-26	2017-10-04	Blue Cube IP LLC	Mixer and reactor and process incorporating the same
CA2893841C (en)	2012-12-18	2018-07-24	Dow Global Technologies Llc	Process for the production of chlorinated propenes
WO2014100039A1 (en)	2012-12-19	2014-06-26	Dow Global Technologies, Llc	Process for the production of chlorinated propenes
US8889929B2 (en) *	2013-02-19	2014-11-18	Honeywell International Inc.	Process to make 1,1,2,3-tetrachloropropene from 1,1,3-trichloropropene and/or 3,3,3-trichloropropene
JP2016507590A (ja)	2013-02-27	2016-03-10	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
WO2014164368A1 (en)	2013-03-09	2014-10-09	Dow Global Technologies Llc	Process for the production of chlorinated alkanes
CN115108882B (zh) *	2022-06-07	2024-04-12	浙江衢化氟化学有限公司	一种1,1,1,2,3-五氯丙烷的连续制备方法
CN117285407A (zh) *	2023-09-25	2023-12-26	广东电网有限责任公司	一种1,1,2-三氯丙烯的制备方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1459842A (fr) *	1964-07-29	1966-06-17	Knapsack Ag	Procédé de préparation de 2-chlorobutène-(2)
GB1152021A (en) *	1965-08-30	1969-05-14	Pullman Inc	Dehydrohalogenation Process

1972
- 1972-12-12 NL NL7216840.A patent/NL160542C/xx not_active IP Right Cessation
- 1972-12-15 DE DE2261516A patent/DE2261516C3/de not_active Expired
- 1972-12-15 BE BE792789D patent/BE792789A/xx not_active IP Right Cessation
- 1972-12-15 GB GB5803872A patent/GB1381619A/en not_active Expired
- 1972-12-15 DD DD167592A patent/DD101140A5/xx unknown
- 1972-12-15 BG BG022127A patent/BG21599A3/xx unknown
- 1972-12-15 YU YU3143/72A patent/YU39903B/xx unknown
- 1972-12-15 RO RO73167A patent/RO60573A/ro unknown
- 1972-12-15 IL IL41101A patent/IL41101A/en unknown
- 1972-12-15 FR FR7244864A patent/FR2169817B1/fr not_active Expired
- 1972-12-15 JP JP47125368A patent/JPS4867209A/ja active Pending
- 1972-12-15 IL IL50070A patent/IL50070A/en unknown
- 1972-12-18 IT IT33069/72A patent/IT974728B/it active
1973
- 1973-06-12 CH CH849373A patent/CH584173A5/xx not_active IP Right Cessation
- 1973-06-12 FR FR7321260A patent/FR2202065A1/fr active Granted
- 1973-06-15 JP JP6697973A patent/JPS5346807B2/ja not_active Expired
1976
- 1976-07-20 IL IL7650070A patent/IL50070A0/xx unknown

Also Published As

Publication number	Publication date
FR2202065B1 (2)	1977-05-06
DE2261516B2 (de)	1979-11-22
NL160542B (nl)	1979-06-15
JPS4867209A (2)	1973-09-13
CH584173A5 (2)	1977-01-31
IL50070A0 (en)	1976-09-30
JPS504006A (2)	1975-01-16
IL50070A (en)	1977-05-31
AU480375A (2)	1974-12-05
NL7216840A (2)	1973-06-19
IL41101A0 (en)	1973-02-28
NL160542C (nl)	1979-11-15
RO60573A (2)	1976-10-15
FR2169817B1 (2)	1977-08-05
IT974728B (it)	1974-07-10
DE2261516C3 (de)	1980-07-31
DD101140A5 (2)	1973-10-20
YU314372A (en)	1982-08-31
DE2261516A1 (de)	1973-06-28
YU39903B (en)	1985-06-30
GB1381619A (en)	1975-01-22
BE792789A (fr)	1973-06-15
BG21599A3 (bg)	1976-07-20
JPS5346807B2 (2)	1978-12-16
FR2202065A1 (en)	1974-05-03
FR2169817A1 (2)	1973-09-14

Publication	Publication Date	Title
IL41101A (en)	1977-05-31	Process for preparing 1,2,3-trichloropropene
US2931840A (en)	1960-04-05	Process for preparing 2, 3, 3, 3-tetrafluoropropene
US3823195A (en)	1974-07-09	Preparation of 1,1,2,3-tetrachloropropene from 1,2,3-trichloropropane
CA1174697A (en)	1984-09-18	Catalytic dehydrohalogenation process
US3214481A (en)	1965-10-26	Process for the halogenation of hydrocarbons
US5689020A (en)	1997-11-18	High temperature chlorination process for the preparation of polychloroolefins
US20030028057A1 (en)	2003-02-06	Methods and materials for the preparation and purification of halogenated hydrocarbons
EP0754170A1 (en)	1997-01-22	Production of pentafluoroethane
EP0002021A1 (en)	1979-05-30	Catalytic dehydrohalogenation process
US5008225A (en)	1991-04-16	Catalytic dehydrohalogenation catalyst
EP0004636B1 (en)	1982-07-07	Process for preparing benzotrifluoride and its derivatives
JP3516322B2 (ja)	2004-04-05	１，１，１，３，３−ペンタフルオロプロパンの脱水方法
US3188356A (en)	1965-06-08	Method for producing vinylidene fluoride
JPS62221639A (ja)	1987-09-29	１，２−ジクロルエタンの製造法
EP0162457B1 (en)	1989-07-26	Catalytic dehydrohalogenation process
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