HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531608Generated: October 25, 2026
Vanillin → 3-Methoxy4-(3-trimethylsilanylpropyloxy)benzaldehyde
https://huagongshe.com/reaction/1531608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Chloropropyl)trimethylsilane | HCID 75362 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxy4-(3-trimethylsilanylpropyloxy)benzaldehyde | HCID 18463172 | 89.1% |
Reaction Steps
3-chloropropyltrimethylsilane (33.14 g, 0.22 mol) was added dropwise over 20 minutes to a mixture of vanillin (30.4 g, 0.2 mol) and potassium carbonate (30.4 g, 0.22 mol) in 150 ml of dry DMF heated to 80° C. under nitrogen. The mixture was maintained for 4 hours at 95°-110° C. The reaction mixture was cooled and poured into ice-cold water. The aqueous phase was extracted three times with dichloromethane. The organic phases were dried over sodium sulfate and concentrated under vacuum. After distillation under vacuum (0.04 mm Hg), 47.5 g (yield: 89%) of 3-methoxy-4-(3-trimethylsilanylpropyloxy) benzaldehyde were obtained in the form of a slightly pinkish oil distilling at 1120-114° C. and employed without further purification in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06200552B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-4b34eb65c568436c86c581bf82f0980b |
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| Source note | uspto-grants-2001_03 |
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