HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982749Generated: October 29, 2026
4-Hydroxybenzoic Acid → 4-(4-Allyloxybutyloxy)benzoic acid
https://huagongshe.com/reaction/1982749
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 solution comprising 14 g of allyl (4-chlorobutyl) ether, 14 g of 4-hydroxybenzoic acid, 14 g of potassium carbonate and 50 ml of dimethylformamide was stirred at 90° C. for 3 hours. Water was added to it, and extracted with toluene, and the toluene layer was well washed with water, and toluene was evaporated away. 20 g of sodium hydroxide, 50 ml of water and 200 ml of ethanol were added to the resulting residue, and refluxed for 2 hours. Ethanol was evaporated away, and hydrochloric acid was added to make it acidic, and then extracted with diethyl ether and dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the resulting residue was recrystallized from a mixed solvent of ethanol and water to obtain 29 g of 4-(4-allyloxybutyloxy)benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07541071B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-651364f736894c24b9436e1b8a8a9c0f |
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| Source note | uspto-grants-2009_06 |
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