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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589838Generated: October 30, 2026

Triethylamine → 3-(Tert-butyldiphenylsilanoxy)-2,2-dimethylpropylamine

https://huagongshe.com/reaction/589838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant1-Propanol, 3-amino-2,2-dimethyl-HCID 117326—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-(Tert-butyldiphenylsilanoxy)-2,2-dimethylpropylamineHCID 8668081072.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution at 0° C. of 0.500 g (4.85 mmol) of 3-amino-2,2-dimethylpropanol (CAS 26734-09-8) in 12 ml of dichloromethane are added 0.059 g (0.48 mmol) of dimethylaminopyridine and 1.35 ml (9.7 mmol) of triethylamine. 1.60 g (5.82 mmol) of tert-butyldiphenylsilyl chloride dissolved in 5 ml of dichloromethane are then added dropwise. The mixture is stirred for 30 minutes at 0° C. and then for 2 hours at room temperature. 20 ml of water are then added. The organic phase is separated out by settling, washed with water and then with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the solvent is evaporated off under reduced pressure to give an oil, which is chromatographed on a column of aminopropyl silica gel, eluting with a mixture of 0 to 10% methanol in dichloromethane, to give 1.20 g of 3-(tert-butyldiphenylsilanoxy)-2,2-dimethylpropylamine in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233965B2
Source datasetuspto-grants-2016_01
ORD IDord-86a38d44fa52433c8a307984a2b4324e
Source noteuspto-grants-2016_01