HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73507Generated: October 29, 2026
Vanillin → 4-(6-Bromo-hexanoyl)-3-methoxy-benzaldehyde
https://huagongshe.com/reaction/73507
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(6-Bromo-hexanoyl)-3-methoxy-benzaldehyde | HCID 86676536 | 80% |
Reaction Steps
An excess of 1,5-dibromopentane (100 g, 3 equivalents) was added to a suspension of vanillin (43) (22 g) and potassium carbonate (30 g) in acetone (700 mL). The reaction mixture was heated at reflux for 2.5 hours and then allowed to stir at room temperature overnight, at which time TLC and LC/MS showed the reaction to be complete. The suspension was subjected to vacuum filtration and the resulting acetone solution was evaporated to dryness under reduced pressure. The residue was applied to a pad of silica gel and washed with 10% ethyl acetate in hexane (2 L) followed by 25% ethyl acetate in hexane to elute the product, removal of excess solvent by rotary evaporation under reduced pressure afforded the product 44 as an oil which crystallised on standing in freezer (35 g, 80% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829184B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-13f308e21ef74714b3722938d9ed1bcc |
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| Source note | uspto-grants-2014_09 |
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