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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525528Generated: October 30, 2026

Imidazole → 5-Bromo-2-((triisopropylsilyloxy)methyl)thiazole

https://huagongshe.com/reaction/525528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
ReactantTriisopropylsilyl chlorideHCID 139400—
Reactant(5-Bromo-1,3-thiazol-2-yl)methanolHCID 11953783—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-((triisopropylsilyloxy)methyl)thiazoleHCID 86695418104%

Reaction Steps

A 100 mL round bottom flask is charged with (5-bromothiazol-2-yl)methanol (2.5 g, 12.9 mmol), imidazole (1.75 g, 25.8 mmol), dimethylformamide (25 mL), and chlorotriisopropylsilane (3.4 mL, 15.5 mmol). The reaction is stirred at room temperature under nitrogen for 72 hours. Contents are diluted with ethylacetate (150 mL), washed with 0.5M hydrochloric acid (2×100 mL) and brine (100 mL), dried (Na2SO4), and concentrated under vacuum to afford the title compound (4.7 g): m/z (Cl) M+H 350+352.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340564B2
Source datasetuspto-grants-2016_05
ORD IDord-d2e18e2e7bbe4b16ab4610f73556121f
Source noteuspto-grants-2016_05