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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370555Generated: November 2, 2026

Cyclohexylamine → 2-chloro-N-cyclohexyl-5-nitrobenzamide

https://huagongshe.com/reaction/1370555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-5-nitrobenzoic acidHCID 17287—
ReactantIsobutyl chloroformateHCID 62365—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product2-chloro-N-cyclohexyl-5-nitrobenzamideHCID 711421—

Reaction Steps

Isobutyl chloroformate (1.43 ml) was added under ice cooling to a solution of 2-chloro-5-nitrobenzoic acid (2.01 g) and triethylamine (1.53 ml) in methylene chloride (40 ml). The mixture was stirred under ice cooling for 45 min. Thereafter, cyclohexylamine (1.25 ml) was added thereto. The reaction solution was stirred at room temperature for 1.5 hr. The precipitated crystals were dissolved in chloroform. The organic layer was washed with water, dilute hydrochloric acid, and water in that order, dried over magnesium sulfate, and then concentrated under the reduced pressure. Ethyl ether was added to the residue. The precipitated crystals were collected by filtration, and then dried to give 2.63 g of N-cyclohexyl-2-chloro-5-nitrobenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583144B2
Source datasetuspto-grants-2003_06
ORD IDord-c881508794534cd5a5b4fc1b851fd3f3
Source noteuspto-grants-2003_06