HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377626Generated: October 27, 2026
Water → 4-Methoxy-3-[6-(4-phenylbut-1-yloxy)hex-1-yloxy]benzaldehyde
https://huagongshe.com/reaction/377626
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Isovanillin | HCID 12127 | — |
| Reactant | 1-[4-[(6-Bromohexyl)oxy]butyl]benzene | HCID 11012439 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Methoxy-3-[6-(4-phenylbut-1-yloxy)hex-1-yloxy]benzaldehyde | HCID 19356267 | 98.9% |
Reaction Steps
To a stirred solution of 3-hydroxy-4-methoxybenzaldehyde (4.8 grams) in dimethylformamide (100 ml) at room temperature is added potassium carbonate (4.9 grams) and 1-bromo-6-(4-phenylbut-1-yloxy)hexane (10.0 grams). After stirring at 80° C. over 4 hours the reaction mixture is poured into water and extracted with ethyl acetate. The combined organics are washed with 1N sodium hydroxide and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The resulting amber oil is filtered through a 5×10 cm pad of silica gel, eluting with a 1:3 mixture of ethyl acetate and hexane, to give 12.0 grams of a colorless oil. MS (m/z) 384.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06028086 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-d9a5e50754914e5992451769dfb68347 |
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| Source note | uspto-grants-2000_02 |
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