HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409342Generated: October 28, 2026
Methyl iodide → (S)-4-Benzyl-3-((S)-2-(4-fluorophenyl)propanoyl)oxazolidin-2-one
https://huagongshe.com/reaction/409342
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | (S)-4-Benzyl-3-(2-(4-fluorophenyl)acetyl)oxazolidin-2-one | HCID 15536019 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-4-Benzyl-3-((S)-2-(4-fluorophenyl)propanoyl)oxazolidin-2-one | HCID 67452410 | 49% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759380B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-5d54573a77b141bd9a481293b2a908ad |
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| Source note | uspto-grants-2014_06 |
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