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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030264Generated: November 2, 2026

2-Aminophenol → 2-(Chloromethyl)-1,3-benzoxazole

https://huagongshe.com/reaction/1030264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
ReactantEthyl 2-chloroethanecarboximidate hydrochlorideHCID 12470659—
SolventEthanolHCID 702—
Product2-(Chloromethyl)-1,3-benzoxazoleHCID 206198965%

Reaction Steps

A mixture of o-aminophenol (4.00 g, 36.6 mmol) and ethyl chloroacetimidate hydrochloride (8.68 g, 54.98 mmol) in ethanol (55 mL) was heated at reflux for 18 hours. The reaction mixture was cooled to room temperature and vacuum filtered. The filtrate was concentrated in vacuo, diluted with methylene chloride and filtered again. The methylene chloride filtrate was dried (MgSO4) and concentrated to afford 3.99 g (65%) of product as a brown oil which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104892
Source datasetuspto-grants-1992_04
ORD IDord-3e0fa8619f6d43a290051e3fc539557d
Source noteuspto-grants-1992_04