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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439306Generated: October 31, 2026

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

https://huagongshe.com/reaction/1439306

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 block. 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 numberUS04058550
Source datasetuspto-grants-1977_11
ORD IDord-90709a3b73d541599a5ed1b0b5d4c205
Source noteuspto-grants-1977_11