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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 726123생성일: 2026년 10월 26일

Vinylidene chloride → 4-Bromo-3-chloro-3,4,4-trifluorobutanoic acid

https://huagongshe.com/reaction/726123

반응식

참여 물질

역할이름HCID투입량
반응물Vinylidene chlorideHCID 6366—
반응물1,2-Dibromo-1-chloro-1,2,2-trifluoroethaneHCID 9634—
반응물3,4,4-Trifluoro-3-butenoic acidHCID 15239174—
반응물Ammonium persulfate sodium formateHCID 86749473—
용매DimethylformamideHCID 6228—
용매Cfc 113HCID 6428—
생성물4-Bromo-3-chloro-3,4,4-trifluorobutanoic acidHCID 10912127—
생성물3,4-Dichloro-3,4,4-trifluorobutanoic acidHCID 21836485—

반응 단계

A new method to prepare the desired 3,4,4-trifluoro-3-butenoic acid (IV) involves a one pot reaction of 1-chloro-1,2-dibromotrifluoroethane (VI) or 1,1,2-trichloretrifluoroethane (X) with vinylidene chloride in the presence of ammonium persulfate/sodium formate/air in DMF to give directly 4-bromo-3-chloro-3,4,4-trifluorobutanoic acid (VIII) or novel compound 3,4-dichloro-3,4,4-trifluoro-butanoic acid (XI). The reaction conditions to prepare XI from X are similar to those described in Hu, Chang-Ming; Qing, Feng-Ling; Zhang, Hong-Gen; J. Fluorine Chem., 1990, (49) 275-280. The formation of XI in the above reaction was confirmed by GC/MS (EI): m/z 212 (M+ 2), 210 (M+), 195, 193, 157, 155, 127, 125, 107, 105, 89, 69, 45. Dehalogenation of VIII or XI with zinc gives IV. ##STR6##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05708032
출처 데이터셋uspto-grants-1998_01
ORD IDord-5b8186e0dd1f42ea92bb9d63f904214c
출처 메모uspto-grants-1998_01