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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431931Generated: November 3, 2026

Methyl bromoacetate → HCID 86585710, compound

https://huagongshe.com/reaction/1431931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant(S)-4-Benzyl-3-hexanoyl-2-oxazolidinoneHCID 10612452—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86585710HCID 86585710—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of N-hexanoyl-4-(S)-benzyloxazolidin-2-one A-2 (7.3 mmol) in THF at −78° C. is added 1.0 M NaHMDS (8.8 mmol) and the reaction stirred at −78° C. for 1 hour. A solution of methyl bromoacetate (8.8 mmol) in THF is then added dropwise, and the resulting mixture is stirred at −78° C. for 1 hour and then at rt overnight. The reaction is quenched with NH4Cl, concentrated, then suspended in EtOAc and washed with 0.5 N HCl and brine, dried and purified by silica gel chromatography (EtOAc/hexanes) to afford the methyl 3-(R)-(n-butyl)-3-[4-(S)-benzyloxazolidin-2-one-3-ylcarbonyl)propionate (A-3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612059B2
Source datasetuspto-grants-2009_11
ORD IDord-8380122c7f21428eb5264a0946a1d997
Source noteuspto-grants-2009_11