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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175680Generated: October 31, 2026

Ethyl bromoacetate → HCID 53212233, compound

https://huagongshe.com/reaction/1175680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-oneHCID 3155599—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53212233HCID 53212233—

Reaction Steps

To a solution of 2-ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one (1.5 mmol, 260 mg) in DMF (2 ml) was added NaH (1.8 mmol, 43 mg) and the reaction mixture was stirred at room temperature for 1 h before the dropwise addition of ethyl bromoacetate (1.5 mmol, 250 mg). The reaction mixture was stirred at room temperature overnight, diluted with water and extracted with ethyl acetate. The organic layer was washed with 1N HCl, Sat. NaHCO3, dried over Na2SO4 and evaporated to dryness. The crude compound was dissolved in MeOH (3 ml) and 1 N NaOH (3 ml) and stirred for 2 h at room temperature. The MeOH was removed under reduced pressure and the resulting aqueous solution extracted with EtOAc. The aqueous layer was acidified to pH 2 with 1N HCl and extracted with EtOAc. The organic phase was dried over Na2SO4 and the solvent was evaporated to give the title compound. LC/MS (10% to 99%): M/Z (M+H)+ (obs)=236; tR=2.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842686B2
Source datasetuspto-grants-2010_11
ORD IDord-bc53b4b1d4f742bab5fe96947ca60b75
Source noteuspto-grants-2010_11