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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969920Generated: October 30, 2026

HCID 57368066, compound → Benzoin

https://huagongshe.com/reaction/969920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57368066HCID 57368066—
SolventChloroformHCID 6212—
ProductBenzoinHCID 8400—

Reaction Steps

As shown in the following reaction 1, 30 g of benzoin acrylate, which is obtained from the reaction of benzoin and chloroacylate, and 1 L of chloroform were added into a 2 L reactor, and was stirred and cooled in iced water. 47 g of 3-chloroperoxybenzoicacid(mCPBA) were slowly added into the cooled solution, and the reaction was carried out at room temperature for 24 hours. After completion of the reaction, the 3-chlorobenzoicacid (by-product) was removed by filtering the product, and then the residual 3-chlorobenzoicacid was removed by washing 2 times with saturated sodium sulfite aqueous solution, 1 time with saturated sodium bicarbonate aqueous solution, 1 time with saturated sodium chloride aqueous solution, and 1 time with distilled water. Next, the product was dried with magnesium sulfate, and chloroform was removed under reduced pressure, and then the product was vacuum dried for 1 day to obtain 27.3 g of the pure benzoin acrylate oxide. NMR spectrum of the obtained benzoin acrylate oxide is described in FIG. 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07309561B2
Source datasetuspto-grants-2007_12
ORD IDord-db40a96cbf6f4165998b4e724bf6acb9
Source noteuspto-grants-2007_12