HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hexamethyldisilazide → HCID 86629985, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-one | HCID 10858190 | — |
| Reactant | HCID 86629984 | HCID 86629984 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86629985 | HCID 86629985 | 41.3% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
Cool a solution of (R)-4-Benzyl-3-pent-4-enoyl-oxazolidin-2-one (0.94 g, 3.6 mmol) in THF (10 mL) to −78° C. Treat this solution dropwise with 10M LiHMDS in THF (4 mL, 4.0 mmol) and stir at −78° C. for 30 minutes. Treat the solution with 1-Chloro-3,4-difluoro-2-iodomethyl-5-trifluoromethyl-benzene (1.35 g, 3.8 mmol) and allowed to slowly warm to room temperature. The reaction stirs 4 hr at room temperature. Quench the reaction with 1N HCl (aqueous) and extracted with Et2O. Wash the organic with brine, dry over MgSO4, filter, and remove the solvent. Purify the crude by silica gel column chromatography using Hexanes:EtOAc to elute the pure product. Remove the solvent to afford 0.725 g (41%) of desired product. MS (m/e): 488 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981918B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-b48129177a3a4a47b9f155feaf4f334c |
| Source note | uspto-grants-2011_07 |