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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217976Generated: October 30, 2026

Ethyl bromoacetate → HCID 58406051, compound

https://huagongshe.com/reaction/217976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantEthyl AcetateHCID 8857—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ProductHCID 58406051HCID 58406051—

Reaction Steps

Sodium hydride (2.5 g) was added to a solution of the compound obtained in Preparation Example 8-(3) (4.15 g) in 1-methyl-2-pyrrolidinone (60 mL) under ice-cooling. The reaction solution was stirred at the same temperature for 30 minutes. Ethyl bromoacetate (10.4 mL) was added dropwise to the reaction solution. The reaction solution was heated to room temperature and stirred at the same temperature for five hours. Saturated aqueous ammonium chloride and ethyl acetate were added to the reaction solution, and the organic layer was separated. The organic layer was washed with aqueous sodium chloride and then dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound (4.77 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198269B2
Source datasetuspto-grants-2012_06
ORD IDord-a8a079e6fba34c9489854b5e03505d25
Source noteuspto-grants-2012_06