HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 20430390, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | SK&F 101055 | HCID 117762 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20430390 | HCID 20430390 | — |
Reaction Steps
A mixture of 0.52 g. of 6-chloro-2,3,4,5-tetrahydro-1H-3-benzazepine, 0.34 g. of allyl bromide, 0.6 g. of potassium carbonate and 20 ml. of 90% ethanol was stirred at room temperature for 17 hours. The mixture was filtered and the filtrate concentrated in vacuo. The residue was extracted with 35 ml. of ether and the ethereal extract treated with isopropanolic hydrogen chloride to precipitate 3-allyl-6-chloro-2,3,4,5-tetra-hydro-1H-3-benzazepine hydrochloride. Recrystallization of this salt from absolute ethanol gave 3-allyl-6-chloro-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride having a melting point of 248°-249°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04496558 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-1f97e5daafc649ff97ba3ac6d55276b7 |
| Source note | uspto-grants-1985_01 |