Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163776Generated: October 31, 2026

Pyridine → 2,3-Dihydroxypropyl-4-hexadecylaminobenzamide

https://huagongshe.com/reaction/2163776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Amino-1,2-propanediolHCID 73561—
ReactantHCID 70506019HCID 70506019—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2,3-Dihydroxypropyl-4-hexadecylaminobenzamideHCID 20437388—

Reaction Steps

A slurry of 8.0 g. of 4-(hexadecylamino)benzoic acid hydrochloride in 175 ml. of CH2Cl2 and 50 ml. of glyme containing 10 ml. of thionyl chloride was heated at reflux for 2 hours. The clear solution was concentrated in vacuo giving 9.5 g. of an amber oil. This oil was diluted with 50 ml. of pyridine containing 0.1 g. of 4-dimethylaminopyridine and 9.1 g. of 3-amino-1,2-propandiol. The reaction was stirred for two days at room temperature. The solution was partitioned between ether and water. The water phase was extracted twice more with 100 ml. of chloroform and ether. The combined organic layer was extracted with water, dried over MgSO4 and evaporated to a tacky solid. The solid was recrystallized from acetone-water and a second time from benzene. A small sample was recrystallized from acetonitrile, m.p. 121°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04136256
Source datasetuspto-grants-1979_01
ORD IDord-e56e52f8e439426ca5dc7ce3590f707e
Source noteuspto-grants-1979_01