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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855761Generated: November 2, 2026

Phenylacetyl chloride → HCID 12837866, compound

https://huagongshe.com/reaction/1855761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 12837860HCID 12837860—
SolventWaterHCID 962—
ProductHCID 12837866HCID 12837866—

Reaction Steps

One-half of the aqueous solution prepared in Step A. above was taken and ice was added while nitrogen was bubbled through the stirred solution. There was then added 4.65 g. (0.03 mole) of phenylacetyl chloride, and after that, with good stirring, there was added over 20 minutes a solution of 1.2 g. (0.03 mole) of sodium hydroxide in 30 ml. of water. Ice was added in intervals while the reaction mixture was stirred an additional hour. The water was then decanted from the solid product, after which it was triturated with cold water and decanted, then triturated with 0.5 ml. of acetic acid in 50 ml. of cold water and decanted. The solid was taken up in dichloromethane, dried, then evaporated to an oil. The oil was triturated with petroleum ether, after which it solidified, yielding 3.2 g. The product was recrystallized from dichloromethane/petroleum ether to yield 2.0 g. This material was chromatographed on a Waters high pressure liquid chromatography apparatus using silica gel and hexane: ethylacetate (2:1) as the eluent. A total of 800 mg. of product was obtained having an m.p. of 123°-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04216160
Source datasetuspto-grants-1980_08
ORD IDord-9c92509bee624cec8f66e0ede51bb56e
Source noteuspto-grants-1980_08