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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629983Generated: November 1, 2026

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

https://huagongshe.com/reaction/1629983

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-butyldiphenyl-silanoxy)-2,2-dimethylpropylamine in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791119B2
Source datasetuspto-grants-2014_07
ORD IDord-49db82e285984f4c8263e260e7840faa
Source noteuspto-grants-2014_07