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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616433Generated: November 1, 2026

Imidazole → tert-Butyl(dimethyl)[(prop-2-yn-1-yl)oxy]silane

https://huagongshe.com/reaction/1616433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPropargyl alcoholHCID 7859—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Solvent1,1-DichloroethaneHCID 6365—
Producttert-Butyl(dimethyl)[(prop-2-yn-1-yl)oxy]silaneHCID 344562267%

Reaction Steps

To an ice cooled stirred solution of prop-2-yn-1-ol (10.0 g, 178.3 mmol) and imidazole (18.2 mg, 267.5 mmol) in dichloroethane (500 mL), was added TBDMSCl (40.24 g, 267.5 mmol) and stirring continued at 0° C. for 1.5 h. On completion, saturated aqueous ammonium chloride solution was added to the reaction mixture and extracted with ethyl acetate (3 times). Combined organic layer was dried over sodium sulphate. Removal of the solvent under reduced pressure followed by solvent washings afforded the desired compound (20 g, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765732B2
Source datasetuspto-grants-2014_07
ORD IDord-6584a8c0e82c470ab52991a244d42512
Source noteuspto-grants-2014_07