Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678702Generated: October 31, 2026

Imidazole → 4-((Tert-butyldimethylsilyl)oxy)-2-fluorobenzonitrile

https://huagongshe.com/reaction/1678702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-Fluoro-4-hydroxybenzonitrileHCID 2734675—
SolventDimethylformamideHCID 6228—
Product4-((Tert-butyldimethylsilyl)oxy)-2-fluorobenzonitrileHCID 5937078273%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Fluoro-4-hydroxybenzonitrile (30.1 g; manufactured by Wako Pure Chemical Industries, Ltd.) and imidazole (18.3 g; manufactured by Tokyo Chemical Industry Co., Ltd.) were dissolved in dehydrated DMF (436 mL; manufactured by Kanto Chemical Co., Inc.), and the solution was cooled to 0° C. Subsequently, TBDMSCl (48.3 g; manufactured by Tokyo Chemical Industry Co., Ltd.) was added thereto, and the mixture was stirred for one hour while the temperature was raised to room temperature. The solvent was evaporated under reduced pressure from the reaction solution, subsequently water was added thereto, and the mixture was extracted two times with ethyl acetate. The organic layer was washed two times with water and with brine, and was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and then the residue was purified by column chromatography (“COLUMN-A.”; n-hexane:ethyl acetate=100:0→94:6). Thus, the title compound (40.3 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008506B2
Source datasetuspto-grants-2011_08
ORD IDord-d59687f4c8524911b17402b0c2ad2e5b
Source noteuspto-grants-2011_08