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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808021Generated: October 30, 2026

Triethylamine → (S)-2-Amino-tert-butyldimethylsilyloxypropane

https://huagongshe.com/reaction/1808021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantL-AlaninolHCID 80307—
SolventDichloromethaneHCID 6344—
Product(S)-2-Amino-tert-butyldimethylsilyloxypropaneHCID 2147473780%

Reaction Steps

A mixture of (S)-(+) 2-amino-1-propanol (1.04 g, 13.85 mmol), tert butyldimethylsilyl chloride (2.09 g, 13.85 mmol) and triethylamine (2 ml, 1.05 eq) was stirred in DCM overnight ca 16 h. The reaction was diluted with DCM, washed with water, satd. NH4Cl, brine, dried and evaporated to an oil. Silica gel purification of the crude using 3% MeOH/CH2Cl2 as eluent provided 2-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-ethylamine (1.76 g, 80%); 1H NMR (300 MHz, CDCl3) 0.0 (s, 6H), 0.82 (s, 9H), 0.99 (d, J=6.5 Hz, 3H), 2.22 (bs, 2H), 2.98 (bs, 1H), 3.30 (dd, J=10 Hz, J=17.0 Hz, 1H), 3.48 (dd, J=10.0 Hz, J=4.3 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357718B2
Source datasetuspto-grants-2013_01
ORD IDord-fae61425203747f380bd0ac483452202
Source noteuspto-grants-2013_01