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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929944Generated: October 27, 2026

Triethylamine → (4S,5S)-4-((tert-Butyldiphenylsilyloxy)methyl)-5-phenyloxazolidin-2-one

https://huagongshe.com/reaction/929944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(4S,5S)-4-Hydroxymethyl-5-phenyl-oxazolidin-2-oneHCID 11116891—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product(4S,5S)-4-((tert-Butyldiphenylsilyloxy)methyl)-5-phenyloxazolidin-2-oneHCID 8671852657.7%

Reaction Steps

To a solution of (4S,5S)-4-hydroxymethyl-5-phenyl-oxazolidin-2-one (3.50 g, 17.2 mmol), NEt3 (4.80 mL, 34.4 mmol), and DMAP (105 mg, 861 μmol) in DMF (20 mL) was added dropwise TBDPSCl (4.86 mL, 18.9 mmol) at room temperature. The reaction was stirred for 3 hours at room temperature. The reaction mixture was then concentrated and diluted with TBME, the organic layers were separated, washed with aqueous NaHCO3 and brine, dried over MgSO4, and concentrated. The residue was purified by column chromatography (120 g SiO2) using EtOAc in heptane from 0% to 60% in order to give the title compound as a white solid (4.28 g, 57%). LC-MS: [M+H] 432.2; Rt 1.36 min; (LCMS method 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296733B2
Source datasetuspto-grants-2016_03
ORD IDord-4f470b8dd2a4424da64fa65619ff1c39
Source noteuspto-grants-2016_03