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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic AcidHCID 135—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloro-4-[(prop-2-en-1-yl)oxy]butaneHCID 13748173—
SolventWaterHCID 962—
Product4-(4-Allyloxybutyloxy)benzoic acidHCID 21960626123%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381350B2
Source datasetuspto-grants-2008_06
ORD IDord-c4e2dfceb9af48f38c8dce42e18a34a7
Source noteuspto-grants-2008_06