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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46650Generated: October 29, 2026

2-(4-Bromophenyl)thiophene → 2-(p-Bromophenyl)-5-(m-nitrophenylthio)thiophene

https://huagongshe.com/reaction/46650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Bromophenyl)thiopheneHCID 7018298—
Reactant1-(Chlorosulfanyl)-3-nitrobenzeneHCID 15620686—
CatalystIronHCID 23925—
SolventCarbon TetrachlorideHCID 5943—
Product2-(p-Bromophenyl)-5-(m-nitrophenylthio)thiopheneHCID 2038665944%

Reaction Steps

To a solution of 21.2 g (0.112 mole) of m-nitrobenzenesulfenyl chloride in 160 ml of carbon tetrachioride were added 24.5 g (0.103 mole) of 2-(p-bromophenyl)thiophene and 0.1 g of iron powder. The reaction mixture was allowed to stand one week at room temperature. Evaporation of the solvent and recrystallization of the residue from 140 ml of ethyl acetate gave 17.6 g (44%) of 2-(p-bromophenyl)-5-(m-nitrophenylthio)thiophene, m.p. 120°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-362563c75c84490c9f528892d920a28b
Source noteuspto-grants-1979_11