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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227085Generated: October 31, 2026

Pyridine → N-(3-Iodophenyl)-4-(tetradecyloxy)benzeneacetamide

https://huagongshe.com/reaction/2227085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-IodoanilineHCID 12271—
Reactantp-TetradecyloxyphenylacetylchlorideHCID 10021844—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-Iodophenyl)-4-(tetradecyloxy)benzeneacetamideHCID 15030163—

Reaction Steps

To a solution of 14.29 g of m-iodoaniline and 15.52 g of pyridine in 150 ml of tetrahydrofuran is added at room temperature over 20 minutes a solution of p-tetradecyloxyphenylacetyl chloride in 150 ml of tetrahydrofuran. The mixture is stirred overnight and the solvent removed. The residue is partitioned between dilute hydrochloric acid and warm chloroform. The separated organic layer is washed with dilute hydrochloric acid, dried and evaporated to a residue which is crystallized from carbon tetrachloride:hexane to give 25.0 g of the desired product as a pink solid, m.p. 108°-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350759
Source datasetuspto-grants-1994_09
ORD IDord-e1155e1c527e471b97ef42acf56463af
Source noteuspto-grants-1994_09