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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735696Generated: October 29, 2026

Methyl iodide → (R)-4-benzyl-3-((R)-2-(4-bromophenyl)propanoyl)oxazolidin-2-one

https://huagongshe.com/reaction/735696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 54374212HCID 54374212—
SolventTetrahydrofuranHCID 8028—
Product(R)-4-benzyl-3-((R)-2-(4-bromophenyl)propanoyl)oxazolidin-2-oneHCID 5402956018%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 76A (380 mg, 1.01 mmol) in THF (5 mL) at −78° C., was added NaHMDS (1.3 mL, 1.0M, 1.3 mmol), dropwise. The solution was stirred at −78° C. for 3 h. A solution of MeI (0.62 mL, 10 mmol) in 2 mL THF was added. The solution was stirred −78° C. for 3 h, and −40° C. for 1 h. The reaction was quenched with sat. NH4Cl and extracted with EtOAc (3×20 mL). The organic layer washed with brine, dried (Na2SO4), and concentrated. Purification via flash chromatography (0-30% EtOAc in hexanes) gives 76B (70 mg, 18%). MS (ESI) m/z 388.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592331B2
Source datasetuspto-grants-2009_09
ORD IDord-65bfaf85709f4008ac9e8bd568a00f96
Source noteuspto-grants-2009_09