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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461935Generated: November 1, 2026

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

https://huagongshe.com/reaction/1461935

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 numberUS05077409
Source datasetuspto-grants-1991_12
ORD IDord-9cb442ad5c074296a2eb3c3025143926
Source noteuspto-grants-1991_12