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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10118Generated: October 26, 2026

4-Hydroxybenzoic Acid → 4-(6-Hydroxyhexyloxy)benzoic acid

https://huagongshe.com/reaction/10118

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic AcidHCID 135—
Reactant6-Chloro-1-hexanolHCID 74828—
SolventPotassium HydroxideHCID 14797—
Product4-(6-Hydroxyhexyloxy)benzoic acidHCID 362841380%

Reaction Conditions

Temperature60 °C

Reaction Steps

Monomers in which the bulky organic group was a t-butyl group and the alkyl groups were hexyl groups were made as follows. 4-hydroxybenzoic acid was dissolved in 30% ethanolic KOH. About 1% of KI was added as a catalyst. The mixture was heated to about 60° C. and a stoichiometric amount of 6-chloro-1-hexanol was slowly added over about ½ hour. After refluxing the reaction mixture for extended period of time (2-15 hrs) the contents was cooled, the reaction mixture was filtered off, and the filtrate solvent was evaporated under vacuum. Water was added into the residue and acidified with HCl and the precipitate was filtered and crystallized with ethanol, yielding approximately an 80% 4-(6-hydroxyhexyloxy)-benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094358B2
Source datasetuspto-grants-2006_08
ORD IDord-dfe4ced729254e01be55cc9bea0175d5
Source noteuspto-grants-2006_08