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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490364Generated: October 30, 2026

Imidazole → Tri-isopropyl-(2-trifluoromethyl-furan-3-ylmethoxy)-silane

https://huagongshe.com/reaction/490364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriisopropylsilyl chlorideHCID 139400—
Reactant(2-Trifluoromethyl-furan-3-yl)-methanolHCID 17953606—
Reactant2-(2-Methylfuran-3-yl)ethan-1-olHCID 18444636—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTri-isopropyl-(2-trifluoromethyl-furan-3-ylmethoxy)-silaneHCID 18444682—

Reaction Steps

A solution of the (2-trifluoromethyl-furan-3-yl)-methanol from (i) in dry dichloromethane (180 ml) was treated with chloro-tri-isopropyl-silane (2.6 g, 13.4 mmoles) and imidazole (1.45 g, 21.3 mmoles) and the mixture was stirred overnight at room temperature. Further aliquots of chloro-tri-isopropyl-silane (0.9 g, 4.64 mmoles) and imidazole (0.5 g, 7.34 mmoles) were added and the mixture was stirred for 3 h. The reaction mixture was diluted with water, the organic phase separated and washed sequentially with 0.1M aqueous hydrochloric acid, water, saturated aqueous sodium bicarbonate, water and brine. After drying, evaporation of the solvents afforded a colourless oil. The oil was distilled under reduced pressure (0.05 torr) in a Kugelruhr apparatus collecting the fraction boiling at an oven temperature of 125±20° C. to afford compound 88 as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528157B2
Source datasetuspto-grants-2009_05
ORD IDord-07ad163b6cf849129ecc6c24c453d60a
Source noteuspto-grants-2009_05