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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537622Generated: October 30, 2026

4-Aminobenzyl alcohol → N-(4-hydroxymethylphenyl) 3,4,5-tris(octadecyloxy)cyclohexylcarboxamide

https://huagongshe.com/reaction/537622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzyl alcoholHCID 69331—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3,4,5-Tris(octadecyloxy)cyclohexylcarboxylic acidHCID 87324385—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductN-(4-hydroxymethylphenyl) 3,4,5-tris(octadecyloxy)cyclohexylcarboxamideHCID 5325732245.4%

Reaction Steps

4-Aminobenzyl alcohol (282 mg, 2.29 mmol) was dissolved in chloroform (40 ml), and HOBt (32 mg, 0.23 mmol) and 3,4,5-tris(octadecyloxy)cyclohexylcarboxylic acid (1.11 g, 1.19 mmol) were added. EDC.HCl (356 mg, 1.86 mmol) and pure water (120 μl) were added under ice-cooling, and the mixture was stirred at room temperature overnight. After completion of the reaction, the solvent was evaporated, and the residue was precipitated with acetonitrile (10 ml), and isolated by silica gel column chromatography (chloroform/ethyl acetate=10:1) to give N-(4-hydroxymethylphenyl) 3,4,5-tris(octadecyloxy)cyclohexylcarboxamide (556 mg, 0.54 mmol, yield 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859732B2
Source datasetuspto-grants-2014_10
ORD IDord-29dfc45e603544b1a8b553917d38fe67
Source noteuspto-grants-2014_10