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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497075Generated: October 25, 2026

Imidazole → (R)-5-(((tert-Butyldimethylsilyl)oxy)methyl)pyrrolidin-2-one

https://huagongshe.com/reaction/497075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinoneHCID 7128291—
SolventDichloromethaneHCID 6344—
Product(R)-5-(((tert-Butyldimethylsilyl)oxy)methyl)pyrrolidin-2-oneHCID 13771167115.1%

Reaction Steps

Imidazole (5.24 g, 77 mmols) was added to a CH2Cl2 (85 ml) solution of (5R)-5-(hydroxymethyl)-2-pyrrolidinone (4.03 g, 35 mmols). Then, during cooling with ice, a CH2Cl2 (15 ml) solution of tert-butyldimethylsilyl chloride (4.53 g, 30 mmols) was added, and the mixture was stirred for 15 hours at room temperature. The solvent was distilled off under reduced pressure, and then the residue was subjected to silica gel column chromatography (SiO2 300 g, MeOH—CHCl3 5:95 v/v) to obtain (5R)-5-[(tert-butyldimethylsilyloxy)methyl]pyrrolidin-2-one (7.92 g, 98.7%):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949553B2
Source datasetuspto-grants-2005_09
ORD IDord-15a1ecbc71dc4a95a037f2d5cec9f155
Source noteuspto-grants-2005_09