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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612579Generated: October 26, 2026

Hydrochloric Acid → 4-(10-Allyloxydecyloxy)benzoic acid

https://huagongshe.com/reaction/1612579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylparabenHCID 7456—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactant10-Iododecyl allyl etherHCID 19797913—
SolventEthanolHCID 702—
Product4-(10-Allyloxydecyloxy)benzoic acidHCID 1979790880%

Reaction Conditions

Temperature80 °C

Reaction Steps

70 mmol (22.7 g) of 10-iododecyl allyl ether, 70 mmol (10.6 g) of methyl p-hydroxybenzoate, and 70 mmol (9.6 g) of potassium carbonate were refluxed in absolute ethanol for 15 hours. After addition of an aqueous potassium hydroxide solution (containing 4.0 g of potassium hydroxide) into the reaction solution, the resulting mixture was further heated at 80° C. for 5 hours. After conclusion of the reaction, the reaction solution was acidified with hydrochloric acid, and the acidified reaction solution was then concentrated under reduced pressure. Water was added to the residue to form a suspension, and the insoluble matter was collected and was then dried, to obtain 18.7 g of 4-(10-allyloxydecyloxy)benzoic acid. (Yield: 80%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190687
Source datasetuspto-grants-1993_03
ORD IDord-84dc5b0f78bb4e8d9ed2b74d4b43b006
Source noteuspto-grants-1993_03