Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365806Generated: November 2, 2026

Imidazole → (S)-3-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)propan-1-ol

https://huagongshe.com/reaction/2365806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(S)-1-(4-chloro-3-fluorophenyl)propane-1,3-diolHCID 86696659—
SolventDichloromethaneHCID 6344—
Product(S)-3-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)propan-1-olHCID 8669666051.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-1-(4-Chloro-3-fluorophenyl)propane-1,3-diol (10.5 g, 51.3 mmol) was dissolved in dichloromethane (200 mL), and imidazole (8.73 g, 128 mmol) was added. The mixture was then cooled to 0° C., and tert-butyldimethylsilyl chloride (9.67 g, 64.1 mmol) was added. The mixture was agitated for 1 hour, diluted with dichloromethane to 250 mL and washed with water, sodium bicarbonate solution, dried and evaporated. Purified by chromatography on silica gel, eluted with 5-10% ethyl acetate/hexanes to give (S)-3-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)propan-1-ol (8.40 g, 26.3 mmol, 51.3% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697715B2
Source datasetuspto-grants-2014_04
ORD IDord-6f3b4cab0e6c490cbcd76f3f05490525
Source noteuspto-grants-2014_04