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HRID 46645作成日:2026年10月25日

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

https://huagongshe.com/reaction/46645

反応式

関与物質

役割名称HCID仕込み量
反応物Diphenyl disulfideHCID 13436—
反応物Benzenesulfenyl chlorideHCID 11008040—
反応物2-(p-Isopropylphenyl)thiopheneHCID 21917177—
触媒IronHCID 23925—
溶媒Carbon TetrachlorideHCID 5943—
生成物2-(p-Isopropylphenyl)-5-(phenylthio)thiopheneHCID 20386666—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04174405
出典データセットuspto-grants-1979_11
ORD IDord-8f80ddcc91a040a0a30d4a6a80130775
出典メモuspto-grants-1979_11