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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732771Generated: October 31, 2026

Pyridine → 1-Chloro-4-{[2-(chloromethyl)phenyl]sulfanyl}-2-methoxybenzene

https://huagongshe.com/reaction/1732771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant{2-[(4-Chloro-3-methoxyphenyl)sulfanyl]phenyl}methanolHCID 12374605—
SolventWaterHCID 962—
Product1-Chloro-4-{[2-(chloromethyl)phenyl]sulfanyl}-2-methoxybenzeneHCID 1237460885%

Reaction Steps

Thionyl chloride (6.5 g) is added dropwise to a stirred mixture of the alcohol from the preceding preparation (11.2 g) and pyridine (4.0 g) at 10°-20° C. The mixture is stirred at room temperature for 3 hours and, after standing overnight, for one additional hour at 30°-40° C. The cooled mixture is decomposed by dropwise addition of water (20 ml) and the product extracted with benzene. The work-up of the extract, followed by crystallization of the crude residue from a small volume of hexane, yields 10.2 g (85%) of 2-(4-chloro-3-methoxyphenylthio)benzyl chloride which in the pure state melts at 57°-59° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238611
Source datasetuspto-grants-1980_12
ORD IDord-0f3014e39cd84df6a31391a9025240a1
Source noteuspto-grants-1980_12