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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748789Generated: October 26, 2026

Imidazole → 4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-ol

https://huagongshe.com/reaction/748789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant2-Butene-1,4-diolHCID 8065—
ReactantEthyl AcetateHCID 8857—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
Product4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-olHCID 6665694942%

Reaction Steps

In a dichloromethane/N,N-dimethylformamide (200 ml/200 ml) mixture were dissolved 2-buten-1,4-diol (10.0 g, 113 mmol) and imidazole (4.70 g, 69.0 mmol), followed by the dropwise addition of t-butylchlorodiphenylsilane (30.0 ml, 115 mmol) at room temperature. After completion of the dropwise addition, the mixture was stirred at room temperature for 4 days. The residue obtained by concentrating the reaction mixture under reduced pressure was added with diethyl ether. From the resulting mixture, the insoluble matter was filtered off. The diethyl ether layer was washed with water and then, the organic layer was dried over anhydrous magnesium sulfate. After fitration, the filtrate was concentrated under reduced pressure. The residue was subjected to flash silica gel chromatography, and the fraction obtained from the hexane:ethyl acetate=2:1 eluate was concentrated under reduced pressure, whereby the title compound (15.3 g, 46.9 mmol, 42%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399775B2
Source datasetuspto-grants-2008_07
ORD IDord-cdac057bba9a459796121b333d8a2070
Source noteuspto-grants-2008_07