HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771145Generated: November 2, 2026
Vanillin → 4-isobutoxy-3-methoxybenzaldehyde
https://huagongshe.com/reaction/1771145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-isobutoxy-3-methoxybenzaldehyde | HCID 673697 | — |
Reaction Steps
In 250 ml three necked flask, equipped with reflux condenser, mechanical stirrer, 30.4 g (200 mmol) of vanillin, 28 g (200 mmol) of dry K2CO3 and 150 ml of abs. dimethylformamide are placed in the flow of argon. The mixture is stirred for 20 min in argon condition, then 34.3 g (250 mmol) of isobutyl bromide is added. The mixture is refluxed with stirring in argon condition for 20 h at 90÷100° C., and concentrated in vacuum at 50÷80° C. to dryness. Then 200 ml of water is added to the residue, the mixture is extracted with (4×100 ml) of dichloromethane. The combined organic fraction is washed with 7% NaOH solution, dried over magnesium sulfate, filtered off, concentrated in vacuum at 50÷80° C. The residue (15 g of brown oil)-crude 4-(2-methylpropyloxy)-3-methoxybenzaldehyde is used on the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249115B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-bdb7e2433d5e4621ab36f3716ba27e03 |
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| Source note | uspto-grants-2016_02 |
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