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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615064Generated: October 26, 2026

Benzyl Chloride → 4-Hydroxy-3-hydroxymethyl-2-pentyl 4-(n-hexadecylamino)benzoate

https://huagongshe.com/reaction/615064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
Reactant3-(Hydroxymethyl)pentane-2,4-diolHCID 61234—
Reactant4-Hexadecylaminobenzoyl chloride hydrochlorideHCID 13255322—
ReactantHCID 178418361HCID 178418361—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-Hydroxy-3-hydroxymethyl-2-pentyl 4-(n-hexadecylamino)benzoateHCID 21326940—

Reaction Conditions

Temperature10 °C

Reaction Steps

A 13.4 g. of 2,4-dihydroxy-3-hydroxymethylpentane solution in dimethoxyethane is added to 2.4 g. of sodium hydride (washed free of mineral oil). After hydrogen evolution ceased, 12.65 g. of benzyl chloride is added and the mixture refluxed for 4 hours. After cooling to 10° C., 24.4 g. of 4-dimethylaminopyridine and 41.6 g. of 4-(n-hexadecylamino)benzoyl chloride hydrochloride are added. Chloroform and water are added after 16 hours and the chloroform extract is dried and evaporated to dryness. The residue is dissolved in acetic acid and hydrogenated at 30 psi hydrogen pressure over palladium black. After filtration and dilution with water, the 4-hydroxy-3-hydroxymethyl-2-pentyl 4-(n-hexadecylamino)benzoate is obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04146546
Source datasetuspto-grants-1979_03
ORD IDord-6d963bd4a3ce435a80c0f0f5b9540ab1
Source noteuspto-grants-1979_03