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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281231Generated: November 2, 2026

Imidazole → (5-Bromothiophen-2-yl)methyl Tert-butyldiphenylsilyl Ether

https://huagongshe.com/reaction/1281231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(5-Bromothiophen-2-yl)methanolHCID 11435467—
SolventDiethyl EtherHCID 3283—
Product(5-Bromothiophen-2-yl)methyl Tert-butyldiphenylsilyl EtherHCID 22393098—

Reaction Steps

Tert-butyldiphenylsilyl chloride (7.8 mL, 30.1 mmol) was added to a solution of 5-bromo(thiophen-2-yl)methyl alcohol (4.9 g, 25.1 mmol) and 9.7 mL of dimethylformamide. The solution was treated with imidazole (4.29 g, 62.8 mmol) and stirred overnight at room temperature. The solution was diluted with ether and washed with 2% aqueous HCl. The layers were separated and the aqueous layer was extracted with ether. The combined organic extracts were washed with brine, and dried (MgSO4), and filtered, and the solvents were removed in vacuo. The residue was purified by silica gel chromatography (hexane) to produce the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06452032B1
Source datasetuspto-grants-2002_09
ORD IDord-084d308304704679b7f195e5c6b58c0f
Source noteuspto-grants-2002_09