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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967413Generated: October 30, 2026

Triethylamine → (R)-tert-Butyldimethyl(oxiran-2-ylmethoxy)silane

https://huagongshe.com/reaction/967413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(-)-GlycidolHCID 6973630—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product(R)-tert-Butyldimethyl(oxiran-2-ylmethoxy)silaneHCID 1100869279.3%

Reaction Conditions

Temperature23 °C

Reaction Steps

tert-Butyl-chloro-dimethylsilane (12.9 g, 85.5 mmol) followed by Et3N (19 mL, 136 mmol) was added to a 0° C. solution of (S)-(+)-glycidol (5.0 g, 67 mmol) in CH2Cl2 (200 mL). The solution was allowed to warm to 23° C. with stirring over 17 h. The resulting pink solution was diluted with Et2O (800 mL) and stirred an additional 30 min. The Et2O layer was washed with saturated aqueous NaHCO3 (200 mL), H2O (2×100 mL), brine (100 mL), dried over Na2SO4 and concentrated. Purification by column chromatography (silica, 5-10% Et2O/hexanes) gave (R)-tert-Butyl-dimethyl-oxiranylmethoxy-silane (10.01 g, 79%). TLC (silica, 10% Et2O/hexanes): Rf=0.5. 1H NMR (CDCl3, 400 MHz): 3.85 (dd, J=11.9, 3.2 Hz, 1H), 3.66 (dd, J=11.9, 4.8 Hz, 1H), 3.09 (m, 1H), 2.77 (dd, J=5.0, 4.2 Hz, 1H), 2.64 (dd, J=5.2, 2.7 Hz, 1H), 0.90 (s, 9H), 0.08 (s, 3H), 0.07 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953793B2
Source datasetuspto-grants-2005_10
ORD IDord-d716d6cf4a4549e492fa3753979829a2
Source noteuspto-grants-2005_10