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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460926Generated: November 2, 2026

4-Hydroxybenzoic Acid → 4-[(10-Hydroxydecyl)oxy]benzoic acid

https://huagongshe.com/reaction/1460926

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic AcidHCID 135—
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Decanol, 10-chloro-HCID 123526—
CatalystPotassium IodideHCID 4875—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-[(10-Hydroxydecyl)oxy]benzoic acidHCID 1976895458%

Reaction Steps

A mixture of 4-hydroxybenzoic acid (69.0 g, 0.5 mol), 10-chloro-1-decanol (106 g, 0.55 mol), potassium hydroxide (75 g, 1.15 mol), potassium iodide (0.1 g), and absolute ethanol (300 mL) was heated to reflux with mechanical stirring for 18 h. The mixture was diluted with water (800 mL) and stirred 0.5 h at room temperature. The mixture was acidified with 12N hydrochloric acid (125 mL) and the mixture stirred for 5 h. The material was allowed to sit overnight and filtered. The solid was washed with water and air dried 4 days. The solid was recrystallized from tetrahydrofuran (300 mL) to give 4-(10-hydroxydecyloxy)benzoic acid (85.2 g, 58%): mp 115°-117° C.; NMR (CDCl3 +d6DMSO) 7.93(d, 2H), 6.85(d, 2H), 4.0(t, 2H), 3.52(t, 2H), 3.48(bs, 1H), 1.9-1.2(m, 16H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05073294
Source datasetuspto-grants-1991_12
ORD IDord-b92e0395dd9344a1b3fcbfa11ed4fcf1
Source noteuspto-grants-1991_12