HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2,3,4,5-tetrahydro-alpha-methyl-1-methyl-1H-1-benzazepine-7-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 19935434 | HCID 19935434 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3,4,5-tetrahydro-alpha-methyl-1-methyl-1H-1-benzazepine-7-methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420273 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-fc8e9b8ab68e43a1a3073916e1d637d1 |
| Source note | uspto-grants-1995_05 |