HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 445035Erstellt: 24. Oktober 2026
3-Hydroxybenzaldehyde → 3-(t-Butyldimethylsilyloxy)benzaldehyde
https://huagongshe.com/de/reaction/445035
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Edukt | Imidazole | HCID 795 | — |
| Edukt | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 3-(t-Butyldimethylsilyloxy)benzaldehyde | HCID 11207111 | 54,1% |
Reaktionsschritte
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 CHCl3 (300 mL) at 0° C. via a funnel. The reaction was stirred under N2 overnight while it warmed to room temperature. The reaction mixture was washed by water (100 mL×3) and brine (100 mL×1), dried over Na2SO4 and concentrated to give crude product (29.56 g), which was purified by column chromatography eluted by (i) pentane and (ii) 3% EtOAc in pentane to give 3-(t-butyl-dimethyl-silanyloxy)-benzaldehyde (21 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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08476280B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-4c8d5becb1184b82ac20379c999b5122 |
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| Quellennotiz | uspto-grants-2013_07 |
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