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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46646Generated: October 28, 2026

Benzenesulfenyl chloride → 2-(m-Chlorophenyl)-5-(phenylthio)thiophene

https://huagongshe.com/reaction/46646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfenyl chlorideHCID 11008040—
Reactant2-(3-Chlorophenyl)thiopheneHCID 12362444—
CatalystIronHCID 23925—
SolventCarbon TetrachlorideHCID 5943—
Product2-(m-Chlorophenyl)-5-(phenylthio)thiopheneHCID 2038660722%

Reaction Steps

A mixture of 89 g (0.46 mole) of 2-(m-chlorophenyl)thiophene, 400 ml of reagent carbon tetrachloride, 54 ml (67 g, 0.46 mole) of benzenesulfenyl chloride and 0.05 g of iron powder was allowed to stand for four days at room temperature. A further 12 ml (15 g, 0.10 mole) of benzenesulfenyl chloride and 0.05 g of iron powder were added. After four days the carbon tetrachloride was removed by distillation. The residue was distilled at reduced pressure to give 30 g (22%) of 2-(m-chlorophenyl)-5-(phenylthio)thiophene, b.p. 200°-205° C. (0.15 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-e3cd56a17f6946528e527b3512c871fa
Source noteuspto-grants-1979_11