Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168055Generated: October 29, 2026

Imidazole → (S)-4-tert-butyldimethylsilyloxy-1-trityloxy-2-butanol

https://huagongshe.com/reaction/1168055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(S)-1-trityloxy-2,4-butanediolHCID 14027585—
SolventDimethylformamideHCID 6228—
Product(S)-4-tert-butyldimethylsilyloxy-1-trityloxy-2-butanolHCID 12114686270.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-1-Trityloxy-2,4-butanediol (1.64 g, 4.7 mmol) and imidazole (0.321 g, 4.715 mmol) were dissolved in DMF (20 ml) and the solution was cooled to 0° C. To the solution was dropped tert-butyldimethylsilyl chloride (0.5 ml, 1.44 mmol, 50% in toluene). After stirring for 1 hour, again to the solution was dropped tert-butyldimethylsilyl chloride (0.5 ml, 1.44 mmol) and the solution was stirred for 1 hour. Further tert-butyldimethylsilyl chloride (0.6 ml, 1.73 mmol) was added to the solution and the solution was stirred over night at room temperature. After dilution with toluene (100 ml), the solution was washed with water (100 ml) twice and saturated brine once, dried on magnesium sulfate, filtered and condensed in vacuo. The residue was subjected to silica gel chromatography to give (S)-4-tert-butyldimethylsilyloxy-1-trityloxy-2-butanol (1.80 g, yield 82.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620977B1
Source datasetuspto-grants-2003_09
ORD IDord-d3834080934048c7b841f232f72039d1
Source noteuspto-grants-2003_09