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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484628Generated: October 25, 2026

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

https://huagongshe.com/reaction/484628

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 numberUS05231182
Source datasetuspto-grants-1993_07
ORD IDord-79eff04e9589476983a7e0fe010c51ff
Source noteuspto-grants-1993_07