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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164064Generated: October 28, 2026

Allyl bromide → HCID 13066667, compound

https://huagongshe.com/reaction/1164064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 5121102HCID 5121102—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 13066667HCID 1306666782.9%

Reaction Conditions

Temperature230 °C

Reaction Steps

A mixture of 4-(2-chlorophenoxy)phenol (15 g), allyl bromide (12.5 g) and potassium carbonate (14 g) in methyl isobutyl ketone (100 ml) was refluxed under heating for 3 hours. After cooling, the reaction mixture was filtered, and the filtrate was evaporated. The residue was dissolved in diethyl ether, washed with dil. aqueous sodium hydroxide and water, dried and evaporated. The oily residue was stirred in a oil bath at 230° C. for 2 hours and distilled to give 2-allyl-4-(2-chlorophenoxy)phenol (14.7 g). bp 189°-192° C./3 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04367238
Source datasetuspto-grants-1983_01
ORD IDord-c43fe311f8bd494c9f86f5d0b50de939
Source noteuspto-grants-1983_01