HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → HCID 21312832, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12668015 | HCID 12668015 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21312832 | HCID 21312832 | — |
Reaction Steps
A mixture of 4.5 g of 6-chloro-7,8-dimethoxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine, 0.02 ml of n-butyl bromide and 0.02 mol of potassium hydroxide is dissolved in 120 ml of dry methanol and refluxed for 48 hours. The reaction mixture is evaporated to dryness, taken up in ethyl acetate and filtered to remove inorganic salts. The filtrate is washed with water, dried and evaporated to give 3-n-butyl-6-chloro-7,8-dimethoxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04160765 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-12f5ef31036c48bd8c99cd5ee2fa7ee3 |
| Source note | uspto-grants-1979_07 |