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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962496Generated: October 27, 2026

4-Nitrobenzoyl chloride → 6,11Dihydro-5-(4-nitrobenzoyl)-5H-dibenz[b,e]azepine

https://huagongshe.com/reaction/962496

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant6,11-Dihydro-5H-dibenz[b,e]azepineHCID 67974—
ReactantDiisopropylethylamineHCID 81531—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product6,11Dihydro-5-(4-nitrobenzoyl)-5H-dibenz[b,e]azepineHCID 5449907796.8%

Reaction Steps

A mixture of 2.34 g (12 mmol) of 6,11-dihydro-5H-dibenz[b,e]azepine, 2.23 g (12 mmol) of 4-nitrobenzoyl chloride, 1.94 g (15 mmol) of diisopropylethylamine and 70.5 mg of 4-(dimethylamino)pyridine in 25 ml of dichloromethane is stirred at room temperature for 2 hours, refluxed for 3 hours and allowed to stand at room temperature for 2 days. The mixture is washed with water, 1N sodium bicarbonate, water, 1N HCl, brine and dried (Na2SO4). The solvent is removed to give 4.0 g of solid. Trituration with ethyl acetate and filtering gives 2.85 g of off-white crystals, m.p. 185°-188° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760031
Source datasetuspto-grants-1998_06
ORD IDord-e259a21c9be04685bfea0cbee256ba39
Source noteuspto-grants-1998_06