Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367158Generated: November 1, 2026

Ethyl bromoacetate → HCID 86616390, compound

https://huagongshe.com/reaction/1367158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 40531003HCID 40531003—
SolventDimethylformamideHCID 6228—
ProductHCID 86616390HCID 86616390—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (2S,5R)-2-methyl-5-phenylmorpholin-3-one from Step E (90 mg, 0.47 mmol) in DMF (2 mL) at 0° C. was added NaH (20 mg of a 60% dispersion in oil, 0.50 mmol). After 10 min, ethyl bromoacetate (79 mg, 0.47 mmol) was added and the mixture was stirred at 0° C. for 2 h. Saturated aqueous NaHCO3 (3 mL) was added and the mixture was extracted with EtOAc (2×30 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—90:10 to 60:40, to give the title compound. MS: m/z=278 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893079B2
Source datasetuspto-grants-2011_02
ORD IDord-4a83a1b4eb7446bb9295df36779c6b8c
Source noteuspto-grants-2011_02