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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

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 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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541071B2
Source datasetuspto-grants-2009_06
ORD IDord-651364f736894c24b9436e1b8a8a9c0f
Source noteuspto-grants-2009_06