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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082172Generated: November 1, 2026

Allyl chloroformate → HCID 22915101, compound

https://huagongshe.com/reaction/1082172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chloroformateHCID 18052—
Reactant4-(Aminomethyl)Benzoic AcidHCID 65526—
SolventSodium HydroxideHCID 14798—
ProductHCID 22915101HCID 2291510164.8%

Reaction Steps

To a solution of 7.55 g of 4-(aminomethyl)-benzoic acid in 50 ml of 1N sodium hydroxide solution were added at 6°-8° C. over 1.5 h 6.55 g of allyl chloroformate. Stirring was continued at 0° C. for 0.5 h and the mixture was then extracted with 60 ml of diethyl ether. The organic phase was extracted with 20 ml of saturated sodium carbonate solution and the combined aqueous layers were then acidified to pH 1.8 by the addition of 12N sulfuric acid and subsequently extracted with ethyl acetate. The ethyl acetate extract was washed with brine, dried over sodium sulfate, and the solvent was evaporated in vacuo. The solid residue was crystallized from ethyl acetate/hexane to yield 7.61 g of 4-(allyloxycarbonylaminomethyl)-benzoic acid as a white solid, m.p. 175°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589473
Source datasetuspto-grants-1996_12
ORD IDord-639cce0405f349069c35c2655b7409db
Source noteuspto-grants-1996_12