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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656602Generated: October 27, 2026

Imidazole → 3-(tert-butyldimethylsilyloxy)dihydrofuran-2(3H)-one

https://huagongshe.com/reaction/656602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactantalpha-Hydroxy-gamma-butyrolactoneHCID 545831—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product3-(tert-butyldimethylsilyloxy)dihydrofuran-2(3H)-oneHCID 5046241100%

Reaction Steps

To a solution of 3-hydroxydihydrofuran-2(3H)-one (5 g, 49 mmol) in anhydrous DMF (50 mL) was added imidazole (6.7 g, 98 mmol) and TBDMS chloride (8.1 g, 54 mmol). The reaction was allowed to stir under an N2 atmosphere at room temperature overnight. The reaction was diluted with diethyl ether and washed with 1 N aqueous HCl×2 then brine×1. The organic phase was dried over Na2SO4 and the solvent removed in vacuo to yield 3-(tert-butyldimethylsilyloxy)dihydrofuran-2(3H)-one (11 g, 49 mmol) as a clear oil. [M+H] calc'd for C10H20O3Si, 217. found, 217.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071766B2
Source datasetuspto-grants-2011_12
ORD IDord-6f7c5d92eaf6472faade91711c2b30bb
Source noteuspto-grants-2011_12