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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276080Generated: October 27, 2026

Sodium Iodide → N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide

https://huagongshe.com/reaction/276080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
ReactantPotassium CarbonateHCID 11430—
ReactantN-1-butanesulfonyl-3-amino-4-nitrobenzamideHCID 18315533—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductN-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamideHCID 1831543452.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution containing 1.10 g of N-1-butanesulfonyl-3-amino-4-nitrobenzamide, 0.273 g of sodium iodide, 1.54 g of potassium carbonate, 2.17 g of 2,4-dichlorobenzyl chloride and 10 ml of methanol was stirred at 60° C. for 24 hours. Further, 2.00 g of 2,4-dichlorobenzyl chloride were added thereto, and the mixture was heated at 60° C. for 36 hours. To the reaction solution were added ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate, and N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide was extracted in the aqueous layer. The organic layer was concentrated to give 0.885 g of N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352985B1
Source datasetuspto-grants-2002_03
ORD IDord-898d436535db481595ac9e4346de175f
Source noteuspto-grants-2002_03