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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244483Generated: October 25, 2026

Imidazole → 2-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-1,3-thiazole

https://huagongshe.com/reaction/244483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1,3-Thiazol-2-ylmethanolHCID 2795213—
SolventDichloromethaneHCID 6344—
Product2-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-1,3-thiazoleHCID 21480592100.9%

Reaction Steps

To a room temperature solution of thiazol-2-ylmethanol (1.00 g, 8.684 mmol) in CH2Cl2 was added imidazole (1.18 g, 17.4 mmol) followed by tert-butyldimethylsilyl chloride (1.70 g, 11.3 mmol). After 30 minutes, the mixture was quenched with 2 mL of MeOH and passed through a pad of silica gel eluting with CH2Cl2 (700 mL) and concentrated in vacuo to afford 2.01 g (100%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658637B2
Source datasetuspto-grants-2014_02
ORD IDord-88ca08a0697a4cb59eae2472cba07378
Source noteuspto-grants-2014_02