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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441223Generated: October 30, 2026

4-Nitrobenzoyl chloride → HCID 22405069, compound

https://huagongshe.com/reaction/441223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantHCID 12206142HCID 12206142—
SolventN,N-DimethylanilineHCID 949—
SolventChloroformHCID 6212—
ProductHCID 22405069HCID 2240506910.9%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 4,4-dimethyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (1.0 g) in N,N-dimethylaniline (20 ml) was added 4-nitrobenzoyl chloride (0.98 g) at ambient temperature. The mixture was stirred at 150° C. for 9 hours. The resulting mixture was diluted with chloroform and the organic layer was washed successively with 1N hydrochloric acid and saturated aqueous sodium bicarbonate. Drying, filtering and the removal of solvents afforded a crude product. The crude product was chromatographed on silica gel (1% methanol in chloroform) to give 4,4-dimethyl-5-(4-nitrobenzoyl)-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (195 mg) as a slightly yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521170
Source datasetuspto-grants-1996_05
ORD IDord-63adbadf001a48bd877468f5c414890f
Source noteuspto-grants-1996_05