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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298041Generated: October 29, 2026

2-Chloro-5-nitrobenzoic acid → N-(1-Adamantylmethyl)-2-chloro-5-nitrobenzamide

https://huagongshe.com/reaction/2298041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitrobenzoic acidHCID 17287—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantTricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
SolventDimethylformamideHCID 6228—
ProductN-(1-Adamantylmethyl)-2-chloro-5-nitrobenzamideHCID 58485280.5%

Reaction Steps

To a solution of 2-chloro-5-nitrobenzoic acid (1.22 g) in N,N-dimethylformamide (1.5 ml) was added carbonyldiimidazole (1.0 g). The resulting reaction mixture was stirred for 2.5 h and then 1-adamantanemethylamine (1.0 g) was added. After 14 h the reaction mixture was partitioned between ethyl acetate and water and the organic layer was separated, washed with water and brine and then dried over sodium sulphate (Na2SO4). The organic layer was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 3-10% methanol in dichloromethane) to yield the subtitle compound as a yellow solid (1.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492355B1
Source datasetuspto-grants-2002_12
ORD IDord-0bcf0fbe11a1434abefa6a423da43c22
Source noteuspto-grants-2002_12