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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401742Generated: November 1, 2026

4-Hydroxybenzoic Acid → 4-(Nonanoyloxy)benzoic acid

https://huagongshe.com/reaction/1401742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic AcidHCID 135—
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantNonanoyl chlorideHCID 69819—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product4-(Nonanoyloxy)benzoic acidHCID 3563821—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

138.1 g (1.0 mol) of para-hydroxybenzoic acid were first dissolved in 500 ml of water and 500 ml of isopropanol and this solution was admixed at 0 to 5° C. with 230.0 g of KOH solution (50% strength by weight aqueous solution, 2.05 mol). The resulting pH was 13.5. Metered into this solution over the course of one hour, then, at 0 to 5° C., were 176.6 g (1.0 mol) of nonanoyl chloride, and the batch was stirred for 30 minutes at 0 to 5° C. thereafter. At the end of the after-stirring, the pH of the reaction mixture was 9.0. The reaction mixture was subsequently adjusted to a pH of 8 at 0 to 5° C. using 25.0 g of HCl solution (32% strength by weight aqueous solution), and the complete solution was heated to 55 to 60° C. and then adjusted to a pH of 1.5 to 3 using 100 g of HCl solution (32% strength by weight aqueous solution). The reaction mixture was cooled to 20 to 25° C. and the solid was filtered off on a suction filter and washed ten times with 150 ml of water. The yield after drying under reduced pressure at 100° C. was 255.95 g (92.0% of theory). According to HPLC and NMR measurement, the product was free from nonanoic acid and from unreacted para-hydroxybenzoic acid. The purity of the product is >99.9% by weight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907118B2
Source datasetuspto-grants-2014_12
ORD IDord-f63d9acebcf9479686ac5bcc926c6f02
Source noteuspto-grants-2014_12