HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497519Generated: October 30, 2026
3-Hydroxybenzaldehyde → 3-(t-Butyldimethylsilyloxy)benzaldehyde
https://huagongshe.com/reaction/497519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(t-Butyldimethylsilyloxy)benzaldehyde | HCID 11207111 | 92.4% |
Reaction Steps
3-Hydroxybenzaldehyde (5.14 g, 42.1 mmol) was added to a suspension of tert-butyl-dimethyl-silyl chloride (6.7 g, 44.4 mmol) and imidazole (3.03 g, 44.5 mmol) in dichloromethane (100 ml) under an atmosphere of nitrogen at room temperature. The reaction mixture was stirred at room temperature for 18 hours, and the mixture washed sequentially with 1 M hydrochloric acid (2-fold 50 ml) followed by a saturated aqueous solution of sodium hydrogen carbonate (50 ml). The organic phase was separated, dried over anhydrous magnesium sulphate and the solvent removed in vacuo. The residual yellow oil was passed through a plug of silica gel eluting with 1:1, by volume, dichloromethane:pentane giving 3-(tert-butyl-dimethyl-silanyloxy)-benzaldehyde (9.2 g) as a golden yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949573B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-e690ce280ca544a89e37cac13711a0e1 |
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| Source note | uspto-grants-2005_09 |
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