HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130269Generated: October 31, 2026
4-Hydroxybenzoic Acid → 4-(4-Allyloxybutyloxy)benzoic acid
https://huagongshe.com/reaction/130269
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Chloro-4-[(prop-2-en-1-yl)oxy]butane | HCID 13748173 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Allyloxybutyloxy)benzoic acid | HCID 21960626 | 123% |
Reaction Steps
A dimethylformamide (50 ml) solution of allyl(4-chlorobutyl) ether 14 g, 4-hydroxybenzoic acid 14 g and potassium carbonate 14 g was stirred at 90° C. for 3 hours. Water was added thereto, and the solution was extracted with toluene. The toluene layer was washed well with water, and then toluene was distilled off. Sodium hydroxide 20 g, water 50 ml and ethanol 200 ml were added to the resulting residue and refluxed for 2 hours. Ethanol was distilled off, and then hydrochloric acid was added to the residue to acidify the solution. The solution was extracted with diethyl ether, and the extract was dried on anhydrous magnesium sulfate. A residue obtained by distilling the solvent off was recrystallized from a mixed solvent of ethanol and water to obtain 29 g of 4-(4-allyloxybutyloxy)benzoic acid. Phase transition temperature: C94N107I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381350B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-c4e2dfceb9af48f38c8dce42e18a34a7 |
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| Source note | uspto-grants-2008_06 |
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