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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37420Generated: October 30, 2026

Methyl iodide → 2,3,4,5-tetrahydro-alpha-methyl-1-methyl-1H-1-benzazepine-7-methanol

https://huagongshe.com/reaction/37420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 19935434HCID 19935434—
SolventDiethyl EtherHCID 3283—
Product2,3,4,5-tetrahydro-alpha-methyl-1-methyl-1H-1-benzazepine-7-methanolHCID 19935399—

Reaction Steps

The Grignard reagent was prepared from 1.04 g of magnesium shavings and 2.30 ml of methyl iodide under argon in 40 ml of absolute ether. To this Grignard solution was slowly added dropwise at room temperature a solution of 4.38 g of 2,3,4,5-tetrahydro-1-methyl-1H-1-benzazepine-7-carboxaldehyde in 10 ml of ether. The reaction mixture was stirred for 2 hours. Thereafter, the mixture was hydrolyzed with saturated ammonium chloride solution, extracted with ether, washed with water and dried. After evaporation, there were obtained 4.47 g of 2,3,4,5-tetrahydro-α-methyl-1-methyl-1H-1-benzazepine-7-methanol as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420273
Source datasetuspto-grants-1995_05
ORD IDord-fc8e9b8ab68e43a1a3073916e1d637d1
Source noteuspto-grants-1995_05