HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230925Generated: October 25, 2026
Vanillin → 3-Methoxy4-(3-trimethylsilanylpropyloxy)benzaldehyde
https://huagongshe.com/reaction/2230925
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 the course of 20 minutes into a mixture of vanillin (30.4 g, 0.2 mol) and potassium carbonate (30.4 g, 0.22 mol) in 150 ml of dry dimethylformamide (DMF) heated to 50° C. under nitrogen. The mixture was maintained for 4 hours at 95°-110° C. The reaction mixture was cooled and poured into ice water. The aqueous phase was extracted 3 times with dichloromethane. The organic phases were dried over sodium sulfate and concentrated in vacuo. After distillation in vacuo (0.04 mm Hg), 47.5 g (yield: 89%) of 3-methoxy4-(3-trimethylsilanylpropyloxy)benzaldehyde were obtained in the form of a slightly pink oil distilling at 112°-114° C. and employed as such in the following step (b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06426428B2 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-a66bf718f9584db2b028a7bd0f7f20bc |
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| Source note | uspto-grants-2002_07 |
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