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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114327Generated: October 25, 2026

2(3H)-Benzoxazolone → Ethyl (2-oxo-1,3-benzoxazol-3(2H)-yl)acetate

https://huagongshe.com/reaction/2114327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(3H)-BenzoxazoloneHCID 6043—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductEthyl (2-oxo-1,3-benzoxazol-3(2H)-yl)acetateHCID 590460103.1%

Reaction Steps

A solution of 1,3-benzoxazol-2(3H)-one (676 mg, 5.0 mmol) in (5 mL) was added to a suspension of NaH (220 mg, 5.5 mmol) in DMF (5 mL) at room temperature, and the resulting solution was stirred for 1 h. Ethyl bromoacetate (0.55 mL, 5.0 mmol) was added to the reaction mixture, and stirring was continued for 2 h. The reaction was quenched with water (10 mL) and extracted with EtOAc (2×20 mL). The organic extracts were combined and washed with water, brine, and dried (Na2SO4). The solvent was removed under reduced pressure to give the title compound (1.14 g, >100%) as a brown solid. MS (ES) m/e 222 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432258B2
Source datasetuspto-grants-2008_10
ORD IDord-6f9c4ab4879644dc9c95565cbb051b37
Source noteuspto-grants-2008_10