HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586921Generated: October 30, 2026
Methyl iodide → 1-methyl-8-nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one
https://huagongshe.com/reaction/1586921
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-Nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one | HCID 4093214 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-methyl-8-nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one | HCID 19760234 | — |
Reaction Steps
2.58 g of 2,3,4,5-tetrahydro-8-nitro-2-oxo-1H-1-benzazepine dissolved in 30 ml of abs. dimethylformamide were added to 650 mg of 55% NaH in 20 ml of abs. dimethylformamide. The mixture was stirred for 1 hour, then cooled to 0° C. and 1.35 ml of methyl iodide were slowly added dropwise thereto. After 45 minutes the mixture was poured on ice, extracted with ethyl acetate, washed with NaCl solution, dried and evaporated. Flash chromatography on silica gel (hexane/ethyl acetate=1/1) yielded 2.46 g of 2,3,4,5-tetrahydro-1-methyl-8-nitro-2-oxo-1H-1-benzazepine as orange crystals of m.p. 151°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05216148 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-289dad2dbe8d4fbdbf1c8cba898583e9 |
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| Source note | uspto-grants-1993_06 |
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