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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763533Generated: October 27, 2026

Potassium Hydroxide → 4-choro-N-[4-(diethylamino)-1-methylbutyl]-2-nitrobenzamide

https://huagongshe.com/reaction/1763533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantNovoldiamineHCID 78953—
Reactant4-Chloro-2-nitrobenzoyl chlorideHCID 10867784—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product4-choro-N-[4-(diethylamino)-1-methylbutyl]-2-nitrobenzamideHCID 13101051—

Reaction Steps

To a vigorously stirred mixture containing 970 g. (6.2 moles) of freshly distilled N1,N1 -diethyl-1,4-pentanediamine, 4 l. of 1,2-dichloroethane and 1 l. of water at 5°-10° C. there was simultaneously added dropwise a solution containing 5.95 moles of 4-chloro-2-nitrobenzoyl chloride in approximately 8 l. of 1,2-dichloroethane and a solution containing 410g. (6.2 moles) of 85% potassium hydroxide in 1 l. of water. When the addition was complete the ice bath was removed and stirring was continued 0.5 hours at room temperature. The organic layer was separated, dried over anhydrous calcium sulfate and evaporated to dryness under vacuum. The residue was dissolved in 3 l. or 1,2-dichloroethane and the resulting solution was treated with decolorizing carbon and filtered. The filtrate was diluted to 6 l. with additional 1,2-dichloroethane to give a pale yellow solution of 4-choro-N-[4-(diethylamino)-1-methylbutyl]-2-nitrobenzamide which was divided into three equal portions which were used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112105
Source datasetuspto-grants-1978_09
ORD IDord-ad936e2dc8c749aab1bbd20354c4c082
Source noteuspto-grants-1978_09