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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777168Generated: November 4, 2026

Chloroacetyl chloride → 5-Hydroxy-2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/1777168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantPotassium CarbonateHCID 11430—
Reactant2-AminoresorcinolHCID 69451—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-Hydroxy-2H-1,4-benzoxazin-3(4H)-oneHCID 4578980764.3%

Reaction Steps

A stirred solution of 2-aminobenzene-1,3-diol (2.0 g, 16.0 mmol) and TEA (1.94 g, 19.2 mmol) in anhydrous DMF (30 mL) was treated with 2-chloroacetyl chloride (1.81 g, 16.0 mmol) and stirring continued for 16 h at room temperature, then K2CO3 (2.65 g, 19.2 mmol) was added and the mixture further stirred for 16 h at the same temperature. The reaction mixture was diluted with DCM (100 mL), washed twice with water and then with brine, dried over anhydrous Na2SO4, filtered and concentrated. The resulting residue was purified by chromatographic column of silicagel to give desired product (1.7 g, 64% yield) LCMS (m/z): 166.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266836B2
Source datasetuspto-grants-2016_02
ORD IDord-bde30a27df5b42fbb9b027981e386b24
Source noteuspto-grants-2016_02