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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492150Generated: November 2, 2026

2-Aminophenol → 2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/1492150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Phenylethylazanium;chlorideHCID 2750517—
SolventChloroformHCID 6212—
Product2H-1,4-benzoxazin-3(4H)-oneHCID 7275732.2%

Reaction Steps

A solution of chloroacetyl chloride (31.2 g) in chloroform (100 ml) was added dropwise to a mixture of 2-aminophenol (25 g), benzylmethylammonium chloride (52.4 g), sodium bicarbonate (77 g) and chloroform (500 ml) which was cooled in an ice-bath. The mixture was stirred for 1 hour and allowed to warm to ambient temperature. The mixture was heated to 55° C. for 5 hours and then stirred at ambient temperature for 16 hours. The mixture was evaporated and the residue was partitioned between ethyl acetate and an aqueous solution of potassium carbonate. The organic phase was washed with dilute aqueous hydrochloric acid and with water, dried (MgSO4) and evaporated. The residue was washed with a mixture of hexane and diethyl ether to leave 3-oxo-2,3-dihydro-4H-1,4-benzoxazine (11 g, 32%) m.p. 172°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05373007
Source datasetuspto-grants-1994_12
ORD IDord-996fe16b080848a784e403139ecb531b
Source noteuspto-grants-1994_12