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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774160Generated: November 1, 2026

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

https://huagongshe.com/reaction/1774160

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 numberUS09259470B2
Source datasetuspto-grants-2016_02
ORD IDord-9edaf30bf2324310a1212f16a7fef5c9
Source noteuspto-grants-2016_02