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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982899Generated: October 26, 2026

Triethylamine → (S)-Glycidoxy-t-butyldimethylsilane

https://huagongshe.com/reaction/982899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(+)-GlycidolHCID 5460455—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(S)-Glycidoxy-t-butyldimethylsilaneHCID 1095430781.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (R)-glycidol (5 g, 67.5 mmol) in dry dichloromethane containing triethylamine (10.3 ml, 74 mmol) cooled down to 0° C., was added a solution of tert-butyldimethylsilyl chloride (11.2 g, 74 mmol) in dry dichloromethane (30 ml). Then DMAP (0.33 g, 2.7 mmol) was added. The mixture was allowed to warm up to room temperature and stirred for 5 hours. The triethylammonium chloride crystals were filtered out and washed with dichloromethane (2×10 ml). The organic solution was washed with brine (2×50 ml) and dried over anhydrous sodium sulfate. The solution was concentrated and passed though a short silica gel column to remove polar impurities, and eluted with hexane/ethyl acetate (3:2). After removing the solvent, a colourless oil was collected and dried in vacuo to provide pure (S)-glycidyl-tert-butyldimethylsilyl ether (10.3 g, 81.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861518B2
Source datasetuspto-grants-2005_03
ORD IDord-c9e87557e12f48259a5223b9db8c55ee
Source noteuspto-grants-2005_03