Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712134Generated: October 25, 2026

Imidazole → Tert-butyl-(2,3-difluoro-benzyloxy)-dimethyl-silane

https://huagongshe.com/reaction/1712134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2,3-Difluorobenzyl AlcoholHCID 447153—
SolventDimethylformamideHCID 6228—
ProductTert-butyl-(2,3-difluoro-benzyloxy)-dimethyl-silaneHCID 1854993375.2%

Reaction Steps

To a solution of (2,3-difluoro-phenyl)-methanol (5.0 g, 35 mmol), imidazole (4.9 g, 72 mmol) and DMF (40 mL) was added tert-butyldimethylchlorosilane (5.4 g, 36 mmol). After stirring at ambient temperature for 24 hours, the mixture was partitioned between 400 mL of ether and 100 mL of water. The organic layer was washed twice with water, dried over MgSO4, filtered and concentrated in vacuo, affording 6.8 g of tert-butyl-(2,3-difluoro-benzyloxy)-dimethyl-silane as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.22 (m, 1H), 7.04 (m, 2H), 4.79 (s, 2H), 0.91 (s, 5H), 0.12 (s, 6H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790902B2
Source datasetuspto-grants-2010_09
ORD IDord-799ce135ff0e4bf98559cd4a41601289
Source noteuspto-grants-2010_09