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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731322Generated: November 2, 2026

2(3H)-Benzoxazolone → 5-(2-Bromopropanoyl)-1,3-benzoxazol-2(3H)-one

https://huagongshe.com/reaction/1731322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(3H)-BenzoxazoloneHCID 6043—
ReactantPropanoyl bromide, 2-bromo-HCID 79047—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
Product5-(2-Bromopropanoyl)-1,3-benzoxazol-2(3H)-oneHCID 1393615850%

Reaction Steps

A mixture of aluminum chloride (40 g) and 2-bromopropionyl bromide (32.4 g) in carbon disulfide (100 ml) was refluxed with stirring for 30 minutes. To the resultant mixture was added 2-benzoxazolinone (13.5 g) and the mixture was refluxed under stirring for 7 hours. The reaction mixture was poured into ice-water and extracted with ethyl acetate. The extract was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo to afford a crystalline residue, which was recrystallized from a mixture of ethyl acetate and diethyl ether to give 5-(2-bromopropionyl)-2-benzoxazolinone (13.5 g). mp. 191°-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04621084
Source datasetuspto-grants-1986_11
ORD IDord-43e94d772bf1493e9e086125c1f97099
Source noteuspto-grants-1986_11