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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46649Generated: October 25, 2026

Benzenesulfenyl chloride → 2-Phenylthio-5-(3,4-xylyl)thiophene

https://huagongshe.com/reaction/46649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfenyl chlorideHCID 11008040—
Reactant2-(3,4-Xylyl)thiopheneHCID 19905009—
CatalystIronHCID 23925—
SolventCarbon TetrachlorideHCID 5943—
Product2-Phenylthio-5-(3,4-xylyl)thiopheneHCID 2038665529.1%

Reaction Steps

A mixture of 37 g (0.197 mole) of 2-(3,4-xylyl)thiophene, 200 ml of reagent carbon tetrachloride, 29 ml (36 g, 0.259 mole) of benzenesulfenyl chloride and 0.05 g of iron powder was allowed to stand two days at room temperature. A vapor phase chromatogram of the mixture showed that all the 2-(3,4-xylyl)thiophene had been consumed. The carbon tetrachloride was removed by distillation and the residue recrystallized from ethanol to give a first crop of 17 g (29%) of 2-phenylthio-5-(3,4-xylyl)thiophene, m.p. 77°-78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-f4ee1ab59c0149929c9669971a4cb76b
Source noteuspto-grants-1979_11