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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218978Generated: October 30, 2026

Imidazole → [1-Benzothien-2-yl(5-bromo-2-fluorophenyl)methoxy](tert-butyl)dimethylsilane

https://huagongshe.com/reaction/218978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantBenzo[b]thiophen-2-yl(5-bromo-2-fluorophenyl)methanolHCID 59281673—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product[1-Benzothien-2-yl(5-bromo-2-fluorophenyl)methoxy](tert-butyl)dimethylsilaneHCID 1845045378%

Reaction Steps

To a dimethylformamide (20 ml) solution of 1-benzothien-2-yl(5-bromo-2-fluorophenyl)methanol (5.0 g) were added imidazole (1.3 g), a catalytic amount of 4-(dimethylamino)pyridine and tert-butyldimethylchlorosilane (2.7 g), followed by stirring at room temperature for 7 hours. To the reaction mixture was added a saturated aqueous ammonium chloride solution, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous ammonium chloride solution and a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain [1-benzothien-2-yl(5-bromo-2-fluorophenyl)methoxy](tert-butyl)dimethylsilane (5.22 g, yield: 78.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198464B2
Source datasetuspto-grants-2012_06
ORD IDord-b371782353b948fd87e7c45898205765
Source noteuspto-grants-2012_06