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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091076Generated: November 2, 2026

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

https://huagongshe.com/reaction/1091076

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 dichloromethane 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 numberUS05084463
Source datasetuspto-grants-1992_01
ORD IDord-47e573eea3134c9a8592f2d0169aa129
Source noteuspto-grants-1992_01