[go: up one dir, main page]

SU1564975A1 - Method of vinyl chloride synthesis - Google Patents

Method of vinyl chloride synthesis

Info

Publication number
SU1564975A1
SU1564975A1 SU4482388/04A SU4482388A SU1564975A1 SU 1564975 A1 SU1564975 A1 SU 1564975A1 SU 4482388/04 A SU4482388/04 A SU 4482388/04A SU 4482388 A SU4482388 A SU 4482388A SU 1564975 A1 SU1564975 A1 SU 1564975A1
Authority
SU
USSR - Soviet Union
Prior art keywords
vinyl chloride
dichloroethane
selectivity
concentration
silica gel
Prior art date
Application number
SU4482388/04A
Other languages
Russian (ru)
Inventor
О.А. Зайдман
Е.И. Верхутова
Ю.А. Трегер
Original Assignee
О.А. Зайдман
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.)
Filing date
Publication date
Application filed by О.А. Зайдман filed Critical О.А. Зайдман
Priority to SU4482388/04A priority Critical patent/SU1564975A1/en
Application granted granted Critical
Publication of SU1564975A1 publication Critical patent/SU1564975A1/en

Links

Landscapes

  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

FIELD: hydrocarbon halides. SUBSTANCE: vinyl chloride is synthesized by dehydrochlorination of 1,2-dichloroethane at 379-390 C in the presence of catalyst cesium chloride applied in the silica gel at concentration 5-11 wt. -% or a mixture of cesium and copper chloride applied on the silica gel at concentration 5-11 and 0.5-11 wt.-% respectively. In this case the conversion of 1,2-dichloroethane reaches 73.77-83.04% selectivity is 99.50-99.71% the yield of vinyl chloride is 73.48-82.98% Work life of catalyst without loss of activity and selectivity is 50-fold as compared with known method. EFFECT: simplified process. 1 tbl
SU4482388/04A 1988-09-15 1988-09-15 Method of vinyl chloride synthesis SU1564975A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU4482388/04A SU1564975A1 (en) 1988-09-15 1988-09-15 Method of vinyl chloride synthesis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU4482388/04A SU1564975A1 (en) 1988-09-15 1988-09-15 Method of vinyl chloride synthesis

Publications (1)

Publication Number Publication Date
SU1564975A1 true SU1564975A1 (en) 1995-08-09

Family

ID=60529152

Family Applications (1)

Application Number Title Priority Date Filing Date
SU4482388/04A SU1564975A1 (en) 1988-09-15 1988-09-15 Method of vinyl chloride synthesis

Country Status (1)

Country Link
SU (1) SU1564975A1 (en)

Similar Documents

Publication Publication Date Title
ATE28853T1 (en) PROCESS FOR THE PREPARATION OF 1,1,2,3TETRACHLOROPROPENE.
UA7138A1 (en) PROCESS FOR PREPARATION OF 1,1,1-trifluoro-2,2- dichloroethane
Hibino et al. Disilylation of acetylenes with silicon-manganese reagent
IL92152A0 (en) Process and intermediates for the preparation of 3,5-dimethyl-4-methoxypyridine derivatives
ES2108296T3 (en) PROCEDURE TO CONVERT 1,1,2-TRICHLOROETHANE TO VINYL AND / OR ETHYLENE CHLORIDE.
SU1564975A1 (en) Method of vinyl chloride synthesis
JPS52136103A (en) Preparation of vinyl chloride
RU95113600A (en) Catalytic process for oxychlorination of ethane to vinyl chloride
DE60208676D1 (en) WATER-INCREASED PRODUCTION OF 1,1,1,3,3-PENTACHLOROPROPANE
FR2408590A1 (en) PEROXIDE PREPARATION PROCESS
JPS52136104A (en) Preparation of vinyl chloride
RU95106778A (en) Use of benzotrichloride as additive during thermal decomposition of dichloroethane
ES8302683A1 (en) Process for the production of ethylene oxide.
MY104604A (en) Use of an aluminosilicate-type catalyst containing gallium in aromatising light cuts containing five to seven carbon atoms per molecule.
GB1451159A (en) Method of purifying hydrogen chloride gas
GB2175895B (en) Preparations of mixtures of 3-phenoxybenzyl bromide and 3-phenoxybenzal bromide
SU1586114A1 (en) Method of vinyl chloride synthesis
Lopez et al. One-pot conversion of α-substituted arylacetaldehydes into α-dicarbonyl compounds
Hargis Free-radical bromination of bromobutane with bromotrichloromethane
SU691186A1 (en) Catalyst for dechlorination of chlorinated olefins
SU1832672A1 (en) Method for production of 1,2-dichloroethane or 1,1,2- trichloroethane
ES2000304A6 (en) Process for the valorization, in the form of perbrominated products, of underbrominated products produced as solutions
DE3665590D1 (en) Method for the preparation of 4'-0-tetrahydropyranyladriamycin b
RO92593B1 (en) Process for preparing 1,1,2-trichloroethane
SU1557955A1 (en) Method of synthesis of benzhydryl chloride