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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371010Generated: October 30, 2026

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

https://huagongshe.com/reaction/1371010

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 numberUS06583155B2
Source datasetuspto-grants-2003_06
ORD IDord-9150266aee404d18b8c37ff32fc99d40
Source noteuspto-grants-2003_06