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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776138Generated: October 26, 2026

4-(Dimethyl-tert-butylsilyl)oxybutan-1-ol → 4-((Tert-butyldimethylsilyl)oxy)butanal

https://huagongshe.com/reaction/1776138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Dimethyl-tert-butylsilyl)oxybutan-1-olHCID 186403—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product4-((Tert-butyldimethylsilyl)oxy)butanalHCID 10888976119.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of PCC (161.5 g, 0.75 mol) in DCM (1000 mL) was added 4-(tert-butyl dimethylsilyl oxy)butan-1-ol (102.0 g, 0.5 mol) in 500 mL of DCM, the mixture was stirred for about 1 hr at 0° C., then was warmed to RT and stirred for 2 hours. Then the mixture was filtered and the filtrate was concentrated in vacuo to give the desired compound of 4-(tert-butyldimethylsilyloxy)butanal (5) (121.2 g, yield 60%) as yellow oil which was purified by column chromatography on silica gel (eluent: PE:EA=50:1). 1H NMR (300 MHz, CDCl3): δ 0.04 (S, 6H), 0.0854 (S, 9H), 1.747 (m, 2H), 3.595 (d, J=12 Hz, 1H), 9.677 (d, J=3.3 Hz, 1H); LC-MC found 203 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265734B2
Source datasetuspto-grants-2016_02
ORD IDord-5bd318a946af4a7ab256ac2e33bd0ad7
Source noteuspto-grants-2016_02