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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520729생성일: 2026년 10월 25일

1,3-Butadiene, 1,2,3,4-tetrachloro- → Hexachlorobutadiene

https://huagongshe.com/reaction/520729

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Butadiene, 1,2,3,4-tetrachloro-HCID 15418—
반응물ChlorineHCID 24526—
반응물1,1,2,2,3,3,4,4-OctachlorobutaneHCID 30117—
촉매Tetrabutylammonium ChlorideHCID 70681—
생성물HexachlorobutadieneHCID 6901—

반응 단계

The present invention is directed to a process for the preparation of of Z-1,1,1,4,4,4-hexafluoro-2-butene from 2,3-dichloro-1,3-butadiene. The process of the present invention includes the sequential steps initiating with initiating the reaction of chlorine with 2,3-dichloro-1,3-butadiene to obtain 1,2,2,3,3,4 hexachlorobutane followed by contacting the 1,2,2,3,3,4 hexachlorobutane with tetrabutyl ammonium chloride in a basic aqueous solution to produce 1,2,3,4-tetrachlorobuta-1,3-diene. Chlorine is added to the 1,2,3,4-tetrachlorobuta-1,3-diene to obtain 1,1,2,2,3,3,4,4 octachlorabutane followed by contacting the 1,1,2,2,3,3,4,4 octachlorobutane with tetrabutyl ammonium chloride in a basic aqueous solution to produce 1,1,2,3,4,4-hexachlorobuta-1,3-diene. Hydrogen fluoride is chlorinated and combined with the 1,1,2,3,4,4-hexachlorobuta-1,3-diene to provide E- or Z-1326mxz (1,1,1,4,4,4-hexafluoro-2-chloro-2-butene). Z-1,1,1,4,4,4-hexafluoro-2-chloro-2-butene is reacted with an aqueous solution of an alkali metal hydroxide and an alkali metal halide in the presence of a quaternary alkylammonium salt having alkyl groups of from four to twelve carbon atoms and mixtures thereof, to produce a mixture including hexafluoro-2-butyne. The final step is hydrogenating hexafluoro-2-butyne to 1,1,1,4,4,4 hexafluro-2-butene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328042B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-8ab912ead069416fbcba6ee870fdce22
출처 메모uspto-grants-2016_05