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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629765Generated: November 1, 2026

Bromoacetyl bromide → HCID 40562710, compound

https://huagongshe.com/reaction/629765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
Reactant(4R)-4-phenyl-1,3-oxazolidin-2-oneHCID 730425—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventAcetone cardiceHCID 18522661—
ProductHCID 40562710HCID 40562710—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (4R)-4-phenyl-1,3-oxazolidin-2-one (100 g, 613 mmol) in THF (2 L) under a nitrogen atmosphere was cooled to −78° C. in dry ice-acetone bath. To the stirred solution was added n-BuLi (337 mL, 2 M solution in cyclohexane, 675 mmol) dropwise over a period of 30 min, followed by the addition of 2-bromoacetyl bromide (123.7 g, 613 mmol) over 15 min. The resulting solution was stirred at 25° C. for 2 h. The reaction was quenched with aqueous NH4Cl (500 mL), and the mixture was extracted three times with EtOAc (3×1 L). The combined organic extracts were washed with water (500 mL) and brine (500 mL), dried (MgSO4), filtered, and the solvent was removed under reduced pressure to give the title compound as a brown solid. The crude product was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315475B2
Source datasetuspto-grants-2016_04
ORD IDord-37cdb8a0b6d24273b5162e730277bf67
Source noteuspto-grants-2016_04