Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484584Generated: October 29, 2026

Pyridine → HCID 9981372, compound

https://huagongshe.com/reaction/484584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Aminobenzyl alcoholHCID 80293—
ReactantHCID 10090356HCID 10090356—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9981372HCID 9981372—

Reaction Steps

To a solution of 10.5 g of 3-(tetradecyloxy)benzeneacetyl chloride in 110 ml of tetrahydrofuran is o added a solution of m-aminobenzyl alcohol in 110 ml of tetrahydrofuran containing 9.05 g of pyridine followed by stirring at ambient temperature for 4 hours and storing in a refrigerator over the weekend. The solvent is evaporated and the residue is poured into water and extracted with tetrahydrofuran:ether. The organic layer is washed with dilute hydrochloric acid, dried and filtered through a pad of magnesium silicate. The filtrate is evaporated and the residue purified by high pressure liquid chromatography using 2:1 hexane:ethyl acetate to give 3.6 g of the desired product as a white powder, m.p. 108°-110° C. and 5.8 g of a white powder, m.p. 86°-90° C. found to be 3-(tetradecyloxy)-[3-[[[3-(tetradecyloxy)phenyl]acetyl]amino]phenyl]benzeneacetic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231182
Source datasetuspto-grants-1993_07
ORD IDord-2462cae18a2746e88b87d5552b9e3345
Source noteuspto-grants-1993_07