HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-4-Benzyl-2-oxazolidinone → (R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-4-Benzyl-2-oxazolidinone | HCID 2734969 | — |
| Reactant | 4-Pentenoyl chloride | HCID 4228493 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-one | HCID 10858190 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
Dissolve (R)-4-Benzyl-2-oxazolidinone (5.906 g, 33.33 mmoles) and 4-Pentenoyl chloride (4.54 g, 38.33 mmoles) in THF (50 mL). Cool the mixture in a dry ice acetone bath, and add n-Butyl Lithium (36.66 mmoles; 14.66 mL; 10.12 g) dropwise at −78° C. Stir the mixture at −78° C. for 30 min and then warm to ambient temperature. Quench the solution with 60 ml of sat. ammonium chloride, and then extract with 60 ml MTBE. Separate the organics and dry over magnesium sulfate. Filter the drying agent and concentrate under vacuum to an oil (6.96 g). LCMS=100% 260 amu (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981918B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-445ebb5b678248ffb3d2c1117c6c1cd5 |
| Source note | uspto-grants-2011_07 |