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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78996Generated: October 29, 2026

Methanol → (S)-2-(tert-Butyl-dimethyl-silanyloxy)-propan-1-ol

https://huagongshe.com/reaction/78996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium borohydrideHCID 4148881—
ReactantEthyl (S)-(-)-2-(tert-butyldimethylsilyloxy)propionateHCID 10966394—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(tert-Butyl-dimethyl-silanyloxy)-propan-1-olHCID 1568806997%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 2M solution of LiBH4 (2.77 g, 0.13 mol) in THF (60 mL) was added dropwise to a solution of (S)-2-(tert-butyl-dimethyl-silanyloxy)-propionic acid ethyl ester (22.75 g, 0.10 mol) and methanol (5.15 mL, 0.13 mol) in diethyl ether (500 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1 hour and then at room temperature for 1.5 hours before cooling to 0° C. and carefully quenching with water. The reaction mixture was filtered and the filtrate extracted with diethyl ether (2×50 mL), the combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo to give the title product as a colourless oil (18.2 g, 97%). 1H NMR (CDCl3, 400 MHz) 3.86-3.77 (1H, m), 3.45-3.37 (1H, m), 3.31-3.22 (1H, m), 1.96-1.85 (1H, m), 1.03 (3H, d, J=6.23 Hz), 0.81 (9H, s), 0.00 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841462B2
Source datasetuspto-grants-2014_09
ORD IDord-5d1588e0d71540deab4e0632e43c9069
Source noteuspto-grants-2014_09