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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256763생성일: 2026년 10월 25일

2-Chloro-1,1,1-trifluoroethane → Benzyl 2,2,2-trifluoroethyl sulfide

https://huagongshe.com/reaction/256763

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-1,1,1-trifluoroethaneHCID 6408—
반응물Benzyl mercaptanHCID 7509—
반응물Sodium HydroxideHCID 14798—
촉매Hexadecyltributylphosphonium bromideHCID 84716—
생성물Benzyl 2,2,2-trifluoroethyl sulfideHCID 273779084%

반응 조건

온도70 °C

반응 단계

A mixture of 1-chloro-2,2,2-trifluoroethane (20 g), benzyl mercaptan (12.4 g, 99% strength), sodium hydroxide (22.0 g of a 22% aqueous solution) and hexadecyl tributyl phosphonium bromide (0.51 g) was charged to a resealable Carius tube under a nitrogen atmosphere and heated at 70° C. for 10 hours. The tube was then cooled to 0° C., unsealed and the contents separated into two layers. The lower organic layer was collected, washed with water and purified by short path distillation to give 2,2,2-trifluoroethylthiomethylbenzene, b.p. 60°-70° C./ 10 mmHg, 17.4 g (yield 84%, strength 99%). The identity of the product was confirmed by gc-mass spectroscopy and nuclear magnetic reconance, and by comparison with data provided in C. Bunyagidj et al, J Org. Chem., 1981, 46 3335.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258547
출처 데이터셋uspto-grants-1993_11
ORD IDord-3a7efd3878424318b295329d78bcf8e4
출처 메모uspto-grants-1993_11