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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013808Generated: November 3, 2026

Lithium Hexamethyldisilazide → (R)-4-Benzyl-3-[(S)-2-(4-benzyloxy-2,6-dimethyl-benzyl)-pent-4-enoyl]-oxazolidin-2-one

https://huagongshe.com/reaction/1013808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-oneHCID 10858190—
Reactant5-(Benzyloxy)-2-(bromomethyl)-1,3-dimethylbenzeneHCID 11426700—
SolventTetrahydrofuranHCID 8028—
Product(R)-4-Benzyl-3-[(S)-2-(4-benzyloxy-2,6-dimethyl-benzyl)-pent-4-enoyl]-oxazolidin-2-oneHCID 6731626878%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Cool a solution of (R)-4-Benzyl-3-pent-4-enoyl-oxazolidin-2-one (4.8 g, 19 mmol) in THF (100 mL) to −78° C. Treat the solution dropwise with 10M LiHMDS in THF (20 mL, 20 mmol) and stir at −78° C. for 30 minutes. Treat the solution with 5-Benzyloxy-2-bromomethyl-1,3-dimethyl-benzene (6.8 g, 22 mmol) and allow to slowly warm to room temperature. The reaction stirs 3 hr at room temperature. Quench the reaction with 1N HCl (aqueous) and extract 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 7.0 g (78%) of desired product. MS (m/e): 484 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981918B2
Source datasetuspto-grants-2011_07
ORD IDord-4656415709bf4fbd8467643569951843
Source noteuspto-grants-2011_07