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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175683Generated: November 1, 2026

Ethyl bromoacetate → HCID 57786461, compound

https://huagongshe.com/reaction/1175683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant2H-1,4-Benzothiazin-3(4H)-one, 2-butyl-HCID 10398598—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57786461HCID 57786461—

Reaction Steps

To a solution of 2-butyl-2H-benzo[b][1,4]thiazin-3(4H)-one (6.3 mmol, 1400 mg) in DMF (5 ml) was added NaH (6.9 mmol, 167 mg) and the reaction mixture was stirred at room temperature for 1 h before the dropwise addition of ethyl bromoacetate (6.3 mmol, 1052 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 (10 ml) and 1 N NaOH (10 ml) and stirred at room temperature for 2 h. 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)=280.2; tR=3.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842686B2
Source datasetuspto-grants-2010_11
ORD IDord-1b4af71c4ebb44e0bec2a8626f08248b
Source noteuspto-grants-2010_11