HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-(Methylthio)-4,5-dihydro-3h-1-benzazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,3,4,5-Tetrahydro-2H-1-benzazepine-2-thione | HCID 12545426 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(Methylthio)-4,5-dihydro-3h-1-benzazepine | HCID 12545428 | — |
Reaction Steps
A solution of Example 182B (2.3 g, 12.97 mmol) in acetone (51.9 mL) was heated to 60° C. in and oil bath. Then potassium hydroxide (36.4 g, 649 mmol) was added followed by the dropwise addition of iodomethane (0.811 mL, 12.97 mmol). The resulting yellow slurry was stirred for 5 minutes and then the solids were collected by filtration. The solids were washed with acetone and the filtrate was concentrated to obtain the crude title compound which was used was used without purification for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846663B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-2880a2dab2a8448fa0f028bf857775c7 |
| Source note | uspto-grants-2014_09 |