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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46651Generated: October 30, 2026

Benzenesulfenyl chloride → 2-p-Anisyl-5-(phenylthio)thiophene

https://huagongshe.com/reaction/46651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfenyl chlorideHCID 11008040—
Reactant2-(4-Methoxybenzyl)thiopheneHCID 11030941—
CatalystIronHCID 23925—
SolventCarbon TetrachlorideHCID 5943—
Product2-p-Anisyl-5-(phenylthio)thiopheneHCID 2038664529%

Reaction Steps

A solution of 34 g (0.179 mole) of 2-p-anisylthiophene in 500 ml of carbon tetrachloride was treated with 23 ml (28.5 g, 0.197 mole) of benzenesulfenyl chloride and 0.1 g of iron powder. The mixture was allowed to stand at room temperature for eight days. The mixture was filtered to remove a small amount of solid. The filtrate was evaporated to give 67 g of crude solid product. Recrystallization from 220 ml of ethyl acetate gave 15.4 g (29%) of 2-p-anisyl-5-(phenylthio)thiophene, m.p. 92°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-b702cd1924054e6f97e089e9f9f5781a
Source noteuspto-grants-1979_11