HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441223Generated: October 30, 2026
4-Nitrobenzoyl chloride → HCID 22405069, compound
https://huagongshe.com/reaction/441223
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | HCID 12206142 | HCID 12206142 | — |
| Solvent | N,N-Dimethylaniline | HCID 949 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22405069 | HCID 22405069 | 10.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521170 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-63adbadf001a48bd877468f5c414890f |
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| Source note | uspto-grants-1996_05 |
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