HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-4-Benzyl-2-oxazolidinone → (S)-4-Benzyl-3-(2-(4-fluorophenyl)acetyl)oxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-4-Benzyl-2-oxazolidinone | HCID 736225 | — |
| Reactant | 4-Fluorophenylacetyl chloride | HCID 3744988 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-4-Benzyl-3-(2-(4-fluorophenyl)acetyl)oxazolidin-2-one | HCID 15536019 | 8,089% |
Reaction Steps
To a cooled (−78° C.) solution of (S)-4-benzyloxazolidin-2-one (10.26 g, 58 mmol, 1.0 equiv) in 100 mL THF was added dropwise n-BuLi (40 mL, 1.6 M, 64 mmol, 1.1 equiv). After stirring for 30 minutes, 4-fluorophenylacetyl chloride (10.0 g, 0.58 mmol, 1.0 equiv) was added dropwise. After stirring for an additional 30 minutes, the reaction mixture was allowed to warm to room temperature. The reaction was quenched with sat'd. aq. NH4Cl, extracted with DCM, and washed with brine. The organic layer was then dried over sodium sulfate, filtered, and concentrated in vacuo. Purification by silica gel (10-20% EtOAc/Hexanes) provided the title compound as a thick oil (14.7 g, 81%). m/z=314.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759380B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-c7cbc2b3080a4eb9b02091749792644b |
| Source note | uspto-grants-2014_06 |