돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46645생성일: 2026년 10월 24일

Diphenyl disulfide → 2-(p-Isopropylphenyl)-5-(phenylthio)thiophene

https://huagongshe.com/ko/reaction/46645

반응식

참여 물질

역할이름HCID투입량
반응물Diphenyl disulfideHCID 13436—
반응물Benzenesulfenyl chlorideHCID 11008040—
반응물2-(p-Isopropylphenyl)thiopheneHCID 21917177—
촉매IronHCID 23925—
용매Carbon TetrachlorideHCID 5943—
생성물2-(p-Isopropylphenyl)-5-(phenylthio)thiopheneHCID 20386666—

반응 단계

Into 150 ml of reagent carbon tetrachloride were added 29 g (0.143 mole) 2-(p-isopropylphenyl)thiophene, 17 ml (21 g, 0.145 mole) of benzenesulfenyl chloride and 0.05 g of iron powder. At the end of four days a vapor phase chromatogram of the reaction mixture showed the presence of diphenyl disulfide, unreacted 2-(p-isopropylphenyl)thiophene and the desired product. An additional 4 ml (5 g, 0.035 mole) of benzenesulfenyl chloride and 0.05 g of iron powder was added and the mixture allowed to stand another four days at room temperature. Evaporation of the carbon tetrachloride gave a residue which was twice recrystallized from 250-ml portions of petroleum ether. There was obtained 16 g (36%) of 2-(p-isopropylphenyl)-5-(phenylthio)thiophene, m.p. 61°-63° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04174405
출처 데이터셋uspto-grants-1979_11
ORD IDord-8f80ddcc91a040a0a30d4a6a80130775
출처 메모uspto-grants-1979_11