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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552043Generated: October 26, 2026

Water → ((2-Chloroethyl)thio)benzene

https://huagongshe.com/reaction/552043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantThiophenolHCID 7969—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product((2-Chloroethyl)thio)benzeneHCID 2170274%

Reaction Steps

Benzenethiol (15.0 g, 0.136 mol) was added to the solution of sodium ethoxide (0.20 mol) in 200 ml of anhydrous ethanol, and the mixture was stirred at room temperature for 15 minutes and then added to the solution of 1-bromo-2-chloroethane in 100 ml of ethanol. The resultant mixture was stirred at room temperature for 3 hours and poured into 300 ml of water. The mixture was extracted three times with ether and the combined organic layer was dried over magnesium sulfate. After removal of the solvent, the compound was purified by flash chromatography using heptane/ethyl acetate (100 to 97/3) as eluent in a yield of 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951550B2
Source datasetuspto-grants-2011_05
ORD IDord-815b378299de4a13abaaa97f6fcc2e5c
Source noteuspto-grants-2011_05