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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013799Generated: October 31, 2026

Lithium Hexamethyldisilazide → HCID 86629985, compound

https://huagongshe.com/reaction/1013799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-oneHCID 10858190—
ReactantHCID 86629984HCID 86629984—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86629985HCID 8662998541.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981918B2
Source datasetuspto-grants-2011_07
ORD IDord-b48129177a3a4a47b9f155feaf4f334c
Source noteuspto-grants-2011_07