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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212359Generated: October 30, 2026

p-Chlorothiophenol → (4-Chlorophenyl)(2,5-difluorobenzyl)sulfane

https://huagongshe.com/reaction/2212359

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ChlorothiophenolHCID 7815—
ReactantTriethylamineHCID 8471—
Reactant2-(Bromomethyl)-1,4-difluorobenzeneHCID 522830—
SolventDichloromethaneHCID 6344—
Product(4-Chlorophenyl)(2,5-difluorobenzyl)sulfaneHCID 1668130475.6%

Reaction Steps

4-Chlorothiophenol (3.6 g, 0.025 mol) in dichloromethane (100 mL) was treated with 2,5-difluorobenzyl bromide (5.17 g, 0.025 mol) and triethylamine (3.9 ml, 0.028 mol). The reaction was stirred for 2 hours then diluted with dichloromethane (250 mL) and washed with water (100 mL) and brine (100 mL). The separated organic layer was dried (MgSO4), evaporated to dryness, and the product purified by passing down a plug of silica eluting with hexane-ethyl acetate mixtures to give 4-chlorophenyl 2,5-difluorobenzyl sulfide (5.12 g). 1H NMR CDCl3 7.23 (4H, s), 6.69–6.86 (3H, m) and 4.04 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101895B2
Source datasetuspto-grants-2006_09
ORD IDord-a08731bc3156449faa00170ae1eed6ef
Source noteuspto-grants-2006_09