HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211571Generated: October 30, 2026
4-Hydroxybenzoic Acid → 4-(4-Allyloxybutyloxy)benzoic acid
https://huagongshe.com/reaction/2211571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Butane, 1,1'-oxybis(4-chloro- | HCID 22800 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Allyloxybutyloxy)benzoic acid | HCID 21960626 | — |
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 thereto, and the liquid was extracted with toluene. The toluene layer was washed well with water, and toluene was distilled off. Sodium hydroxide 20 g, water 50 ml and ethanol 200 ml were added to the resulting residue, and the solution was refluxed for 2 hours. Ethanol was distilled off, and hydrochloric acid was added to acidify the solution. It was extracted with diethyl ether and dried on anhydrous magnesium sulfate. The solvent was distilled off, and a residue thus obtained was recrystallized from a mixed solvent of ethanol and water to obtain 29 g of 4-(4-allyloxybutyloxy)benzoic acid. Phase transition temperature: C 94 N 107 I
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07101595B2 |
|---|
| Source dataset | uspto-grants-2006_09 |
|---|
| ORD ID | ord-092cbb788c544e129f2ca9fbba18a7fd |
|---|
| Source note | uspto-grants-2006_09 |
|---|