HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 8-Bromo-2,3,4,5-tetrahydro-1-benzothiepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 8-bromo-3,4-dihydro-2H-benzo[b]thiepin-5-one | HCID 22337456 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | 8-Bromo-2,3,4,5-tetrahydro-1-benzothiepine | HCID 19935404 | 72.5% |
Reaction Steps
15.6 g of 8-bromo-3,4-dihydro-1-benzothiepin-5(2H)-one were dissolved in 70 ml of diethylene glycol. The solution was treated with 6.55 ml of hydrazine hydrate and 7.5 g of solid potassium hydroxide and heated to 180°-190° C. under reflux for about 30 hours. After cooling, the mixture was poured on to ice and extracted with ether. The organic phase was washed with water, dried and evaporated. Chromatography on silica gel with petroleum ether yielded 10.7 g of 8-bromo-2,3,4,5-tetrahydro-1-benzothiepine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05037825 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-487dd84cbe2540cbbe46ae0e34f3cfda |
| Source note | uspto-grants-1991_08 |