Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903468Generated: November 2, 2026

Benzyl Bromide → 4-Benzylthio-2,3-dichloroanisole

https://huagongshe.com/reaction/1903468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Dichloro-4-methoxybenzene-1-thiolHCID 15914269—
SolventDimethylformamideHCID 6228—
Product4-Benzylthio-2,3-dichloroanisoleHCID 1329019387.5%

Reaction Steps

A solution of 6.23 g of 2,3-dichloro-4-methoxythiophenol in 60 ml of sieved-dried dimethylformamide is added to 0.75 g of sodium hydride over a period of 2-3 minutes. After stirring at room temperature for 20 minutes, the yellowish solution is treated with 5.10 g of benzyl bromide at a rate so that the temperature does not rise above 40°. Stirring is continued for an additional 30 minutes. The cloudy mixture is poured onto 200 g of crushed ice with caution and the white precipitate is collected on a filter after 1 hour at 10° C. The air-dried product is recrystallized from acetone-hexane to give 7.8 g of 4-benzylthio-2,3-dichloroanisole as white needles, mp 116°-117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436748
Source datasetuspto-grants-1984_03
ORD IDord-9979d9b41949412cb1903d4f9a2ea1cd
Source noteuspto-grants-1984_03