HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929648Generated: October 31, 2026
3-Hydroxybenzaldehyde → 3-(t-Butyldimethylsilyloxy)benzaldehyde
https://huagongshe.com/reaction/929648
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(t-Butyldimethylsilyloxy)benzaldehyde | HCID 11207111 | 54.1% |
Reaction Steps
t-Butyldimethylchlorosilane (26.01 g; 172.56 mmol) was added to a solution of 3-hydroxybenzaldehyde (20.7 g; 164.35 mmol) and imidazole (27.97 g; 410.9 mmol) in chloroform (300 mL) under nitrogen at 0° C. The reaction was allowed to warm to room temperature and stirred overnight. The reaction mixture was washed with water (100 mL×3) and brine (100 mL), dried over anhydrous sodium sulfate and concentrated to give crude product (29.56 g), which was purified by column chromatography on silica gel eluting with (i) pentane and (ii) 3% ethyl acetate in pentane to give 3-(t-butyl-dimethylsilanyloxy)benzaldehyde (21.0 g; 54%). 1H NMR (300 MHz, CDCl3) δ 9.93 (s, 1H), 7.45 (d, 1H, J=7.5 Hz), 7.38 (dd, 1H, J=7.5, 7.5 Hz), 7.31 (d, 1H, J=1.0 Hz), 7.09 (1H, dd, J=7.5, 1.0 Hz), 0.98 (s, 9H), 0.20 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296707B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-003a1ebada8b4f928374cc0736fbcd94 |
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| Source note | uspto-grants-2016_03 |
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