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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic AcidHCID 135—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantButane, 1,1'-oxybis(4-chloro-HCID 22800—
SolventWaterHCID 962—
Product4-(4-Allyloxybutyloxy)benzoic acidHCID 21960626—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101595B2
Source datasetuspto-grants-2006_09
ORD IDord-092cbb788c544e129f2ca9fbba18a7fd
Source noteuspto-grants-2006_09