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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922694Generated: October 30, 2026

Methyl iodide → (S)-4-Benzyl-3-((S)-2-(4-fluorophenyl)propanoyl)oxazolidin-2-one

https://huagongshe.com/reaction/922694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant(S)-4-Benzyl-3-(2-(4-fluorophenyl)acetyl)oxazolidin-2-oneHCID 15536019—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-Benzyl-3-((S)-2-(4-fluorophenyl)propanoyl)oxazolidin-2-oneHCID 6745241049%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a room-temperature solution of (S)-4-benzyl-3-(2-(4-fluorophenyl)acetyl)oxazolidin-2-one (5.1 g, 16.3 mmol, 1.0 equiv) in dry THF (100 mL) was added iodomethane (1.0 mL, 16.2 mmol, 1.0 equiv) by syringe. The resulting mixture was cooled to −78° C., and NaHMDS (8.15 mL, 2M in THF, 16.3 mmol, 1.0 equiv) was added dropwise by syringe. After stirring for 15 minutes at −78° C., the reaction mixture was allowed to warm to room temperature. The reaction was quenched with sat'd. aq. NH4Cl, and diluted with EtOAc. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification by silica gel chromatography (7-20% EtOAc/Hexanes) provided the title compound (2.6 g, 49%). m/z=328.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278962B2
Source datasetuspto-grants-2016_03
ORD IDord-232144605e534c29a27906b9003b6293
Source noteuspto-grants-2016_03