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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853896Generated: November 1, 2026

Methyl iodide → HCID 68229193, compound

https://huagongshe.com/reaction/1853896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 86689559HCID 86689559—
SolventTetrahydrofuranHCID 8028—
SolventSodium BisulfateHCID 516919—
ProductHCID 68229193HCID 6822919345.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (S)-4-benzyl-3-(2-(4-bromo-2-fluorophenyl)acetyl)oxazolidin-2-one (3.6 g, 9.2 mmol) in THF (40 mL) was added a solution of methyl iodide (1 M solution in toluene, 9.6 mL, 9.6 mmol). The mixture was cooled to −78° C. and a solution of sodium bis(trimethylsilyl)amide (1 M in THF, 9.6 mL, 9.6 mmol) was added dropwise. The resultant dark red mixture was stirred for 15 min at ca. −78° C. and allowed to warm up to room temperature. After 3.5 h the reaction mixture was diluted with saturated aqueous sodium bisulfate (ca. 20 mL), and extracted with ethyl acetate (1×50 mL). The extract was washed with brine (2×50 mL), dried over sodium sulfate, and evaporated under vacuum. Flash chromatography of the residue afforded the desired product (1.7 g, 45%) as light yellow solid: ESI MS m/z 407 [C19H17BrFNO3+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962648B2
Source datasetuspto-grants-2015_02
ORD IDord-d12ad6c6c74e4f91b5efb74a70305aef
Source noteuspto-grants-2015_02