Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891037Generated: October 30, 2026

Imidazole → 4-((Tert-butyldimethylsilyl)oxy)but-2-yn-1-ol

https://huagongshe.com/reaction/891037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
Reactant2-Butyn-1-olHCID 12991—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDiethyl EtherHCID 3283—
Product4-((Tert-butyldimethylsilyl)oxy)but-2-yn-1-olHCID 5461845—

Reaction Conditions

Temperature22 °C

Reaction Steps

A solution of 175 g of tert-butyldimethylsilyl chloride in 100 ml of a 1:1 mixture that consists of hexane and dimethylformamide is slowly added in drops at 0° C. under nitrogen to a solution of 100 g of 2-butin-1-ol and 158 g of imidazole in 300 ml of dimethylformamide, and it is stirred for 2 hours at 0° C. and for 16 hours at 22° C. The reaction mixture is diluted with 2.5 l of ether, washed once with water, once with 5% sulfuric acid, once with water, once with saturated sodium bicarbonate solution and washed neutral with semi-saturated sodium chloride solution. After drying on sodium sulfate and filtration, it is concentrated by evaporation in a vacuum. The residue that is thus obtained is purified by chromatography on silica gel. With hexane/0–40% ether, 74.3 g of the title compound is obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001916B1
Source datasetuspto-grants-2006_02
ORD IDord-5ab7c7dd027846f3b88a090e622a767a
Source noteuspto-grants-2006_02