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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26356Generated: October 25, 2026

Triethylamine → 4-Ethyl-3-o-chlorobenzoyl-4-oxazolin-2-one

https://huagongshe.com/reaction/26356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chlorobenzoyl chlorideHCID 69110—
Reactant4-Ethyloxazol-2(3H)-oneHCID 21322953—
SolventBenzeneHCID 241—
Product4-Ethyl-3-o-chlorobenzoyl-4-oxazolin-2-oneHCID 21322955—

Reaction Steps

A solution of o-chlorobenzoyl chloride (1.93 g.) and 4-ethyl-4-oxazolin-2-one (1.13 g.) in 30 ml. of benzene is cooled to 10° C. and reacted with 1.21 g. of triethylamine dissolved in 5 ml. of benzene. The reaction mixture is stirred at room temperature for 1 hour. The excess triethylamine and benzene is removed under reduced pressure to leave a light yellow oil (2.4 g.) which is triturated with ethanol whereupon a crystalline solid separates. The solid is removed and washed with a small amount of cold ethanol and dried. Yield 0.3 g.; m.p. 110°-112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150030
Source datasetuspto-grants-1979_04
ORD IDord-b8b94529bf3a4d078af2c164c5aa785e
Source noteuspto-grants-1979_04