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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164075Generated: October 28, 2026

Allyl bromide → 2-(2-Chlorophenylthio)-6-allylphenol

https://huagongshe.com/reaction/1164075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Chlorophenylthio)phenolHCID 20513469—
SolventMethyl Isobutyl KetoneHCID 7909—
Product2-(2-Chlorophenylthio)-6-allylphenolHCID 1306666883.5%

Reaction Steps

A mixture of 2-(2-chlorophenylthio)phenol (33 g), allyl bromide (25 g) and dried potassium carbonate (29 g) in methyl isobutyl ketone (200 ml) was refluxed under heating for 1.5 hours. After cooling to the ambient temperature, the reaction mixture was filtered, and the filtrate was evaporated under reduced pressure. The resultant oily residue was stirred at 230° C. for 3 hours and then distilled under reduced pressure to give oily 2-(2-chlorophenylthio)-6-allylphenol (32.2 g) bp 157°-162° C./0.7 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04367238
Source datasetuspto-grants-1983_01
ORD IDord-e1215f4f06b9471583ca78ed7edf3cc8
Source noteuspto-grants-1983_01