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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505210Generated: October 30, 2026

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

https://huagongshe.com/reaction/1505210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantPotassium CarbonateHCID 11430—
Reactant2-AminoresorcinolHCID 69451—
SolventDimethylformamideHCID 6228—
Product5-Hydroxy-2H-1,4-benzoxazin-3(4H)-oneHCID 4578980721%

Reaction Steps

TEA (3.34 ml, 2 equiv.) and after chloroacetyl chloride (1.15 ml, 1.2 equiv.) were added dropwise to a solution of commercially available 2-aminobenzene-1,3-diol (1.5 g, 11.99 mmol) in 20 ml of DMF. After one hours of stirring at room temperature, K2CO3 (3.3 g, 2 equiv.) was added and the reaction was stirred at room temperature overnight. The solvent was evaporated and to the residue water was added. After filtration, the solid material was washed with MeOH and diethyl ether giving 410 mg of a grey solid. Yield=21% 1HNMR (DMSO, 200 MHz) δ 3.47 (1H, bs), 4.47 (2H, s), 6.44 (2H, m), 6.72 (1H, t, J=8 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216975B2
Source datasetuspto-grants-2015_12
ORD IDord-d696600dc803456583d9c3c8fefcbe2e
Source noteuspto-grants-2015_12