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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249589Generated: November 2, 2026

Allyl Alcohol → Allyl 2-chlorobenzoate

https://huagongshe.com/reaction/1249589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantTriethylamineHCID 8471—
Reactant2-Chlorobenzoyl chlorideHCID 69110—
SolventChloroformHCID 6212—
ProductAllyl 2-chlorobenzoateHCID 348480—

Reaction Steps

Sixty parts of allyl alcohol were dissolved in 240 parts of chloroform, followed by an addition of 105 parts of triethylamine. While stirring the resultant mixture at 10°-15° C., 175 parts of o-chlorobenzoyl chloride were added dropwise over 2 hours. After the resultant mixture was heated at 45°-50° C. for 3 hours, the liquid reaction mixture was poured in a separation funnel and washed first with dilute hydrochloric acid and then with water. The thus-formed light-yellowish organic layer was dried with calcium chloride and then treated with activated carbon. After driving chloroform off, the residue was distilled under reduced pressures to obtain 153 parts of allyl o-chlorobenzoate (hereinafter called "Compound A"; b.p. 101° C./3.5 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632969
Source datasetuspto-grants-1986_12
ORD IDord-81a57e085f734fdd84ee2817ce9e0fe4
Source noteuspto-grants-1986_12