Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611241Generated: October 31, 2026

Methyl bromoacetate → HCID 86585710, compound

https://huagongshe.com/reaction/1611241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 10612452HCID 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 numberUS06987104B2
Source datasetuspto-grants-2006_01
ORD IDord-9e3d21b8fdc54129ab46491dfad36f23
Source noteuspto-grants-2006_01