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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409243Generated: October 30, 2026

Pyridine → HCID 44203196, compound

https://huagongshe.com/reaction/2409243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-Chloro-2-nitroanilineHCID 74218—
ReactantBenzoyl chloride, 2-chloro-5-nitro-HCID 117637—
SolventDichloromethaneHCID 6344—
ProductHCID 44203196HCID 4420319686.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Chloro-2-nitroaniline (1 g; 5.8 mmol) and pyridine (0.64 ml; 8.1 mmol) were dissolved in dichloromethane (10 ml) and cooled to 0° C. This was added dropwise over 5 minutes to a solution of 2-chloro-5-nitrobenzoyl chloride (1.34 g; 6.1 mmol) in dichloromethane (5 ml). The reaction was stirred at room temperature for 72 hours before adding further acid chloride (1.34 g) and pyridine (0.64 ml). After 30 minutes, the solvent was evaporated and the bisacylated residue treated with 1:1 concentrated ammonia/acetonitrile (10 ml). All the solvent was removed after 5 minutes and the residue crystallised from 1:1 chloroform/heptane (30 ml) to give 2-chloro-N-(5-chloro-2-nitro-phenyl)-5-nitro-benzamide (1.78 g, 86%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815895B2
Source datasetuspto-grants-2014_08
ORD IDord-0f27140f54c84aa591a6eb6f6f6c4171
Source noteuspto-grants-2014_08