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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518845Generated: October 30, 2026

Methyl iodide → 1-methyl-8-nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one

https://huagongshe.com/reaction/518845

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 Steps

144 mg of NaH (50%) are added to a solution of 549 mg of 8-nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one in 15 ml of DMF. The reaction medium is stirred for 15 minutes and then 187 μl of iodomethane are added. The mixture is stirred for 16 hours at ambient temperature and then run into ice-cold water and extracted with ethyl acetate. The organic phase is washed with a saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue is taken up in diisopropyl ether and the insoluble material is filtered off and dried under vacuum, so as to give 405 mg of 1-methyl-8-nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one in the form of a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115140B2
Source datasetuspto-grants-2015_08
ORD IDord-b6bdb8e60a454b369e50a6024c4a041c
Source noteuspto-grants-2015_08