HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760895Generated: October 31, 2026
Vanillin → 4-(Dodecyloxy)-3-methoxybenzaldehyde
https://huagongshe.com/reaction/1760895
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | 1-Bromododecane | HCID 8919 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Dodecyloxy)-3-methoxybenzaldehyde | HCID 287532 | — |
Reaction Steps
Vanillin (100 g; 0.657 mol) is dissolved in ethanol (500 ml), and dried K2CO3 (101.5 g; 0.73 mol) is added. Heating to 80° C. is then carried out and 1-bromododecane is added dropwise under a protective gas atmosphere. The suspension is heated at reflux for a further 16 hours. After cooling to 25° C., filtration is carried out, the residue is then washed several times with ethanol and the combined filtrates are concentrated to dryness by evaporation. The residue is dissolved in tert-butyl methyl ether. Washing is then carried out with 1M aqueous sodium hydroxide solution (3×200 ml) and water (1×200 ml), and the organic phase is dried over Na2SO4, filtered off and concentrated to dryness by evaporation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06846492B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-d60aaa8b09d0487e813bb6b3bf4cb49e |
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| Source note | uspto-grants-2005_01 |
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