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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27667Generated: October 26, 2026

Sodium Iodide → N-[(4-Chlorophenyl)methyl]-N-(5-phenylthiophen-2-yl)benzamide

https://huagongshe.com/reaction/27667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantSodium hydrideHCID 24758—
ReactantN-(5-Phenyl-2-thienyl)-benzamideHCID 23341604—
SolventDimethylformamideHCID 6228—
ProductN-[(4-Chlorophenyl)methyl]-N-(5-phenylthiophen-2-yl)benzamideHCID 2334161551.2%

Reaction Steps

The amide of Example 53 (2.8 g, 0.01 mole) in dimethylformamide (25 ml.) was added to sodium hydride (0.0105 mole) (from 40-50% NaH in oil, 0.74 g) which was stirred in dimethylformamide (25 ml.) and cooled in ice. The mixture was stirred for 0.5 hr. and treated with a solution of p-chlorobenzyl chloride (3.22 g, 0.02 mole) in DMF (15 ml.) and a trace of NaI. The mixture was stirred, initially at ice-bath temperature and them at room temperature overnight and then refluxed for 3 hours to complete the reaction. The DMF was evaporated off, water was added, the product extracted with chloroform, which was dried (Na2SO4), filtered and evaporated to give the N-p-chlorobenzyl-benzamide (2.07 g.) as a viscous oil, b.p. 240°-245° C./0.35 mm.Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04222946
Source datasetuspto-grants-1980_09
ORD IDord-addf2b9ec90943a3879b3d89bdf657d3
Source noteuspto-grants-1980_09