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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant8-Nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-oneHCID 4093214—
SolventDimethylformamideHCID 6228—
Product1-methyl-8-nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-oneHCID 19760234—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05216148
Source datasetuspto-grants-1993_06
ORD IDord-289dad2dbe8d4fbdbf1c8cba898583e9
Source noteuspto-grants-1993_06