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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Dimethyl-tert-butylsilyl)oxybutan-1-ol | HCID 186403 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-((Tert-butyldimethylsilyl)oxy)butanal | HCID 10888976 | 119.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09265734B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-5bd318a946af4a7ab256ac2e33bd0ad7 |
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| Source note | uspto-grants-2016_02 |
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