HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 802757, compound → HCID 19974016, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 802757 | HCID 802757 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19974016 | HCID 19974016 | — |
Reaction Steps
A solution of 55 parts of the ether obtained in the preceding paragraph in 800 parts of ethanol is hydrogenated over Raney nickel catalyst at room temperature and atmospheric pressure. When hydrogen uptake ceases the catalyst is removed by filtration and the ethanol solvent is evaporated. The residue is then dissolved in 500 parts by volume of hexane, filtered, and then cooled. There is then obtained yellowish-white crystals which are separated by filtration to give 8-trifluoromethyl-dibenz[b,f][1,4]oxazepine melting at about 86°-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05604220 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-384cf096dacd457eb05c0e17e700b735 |
| Source note | uspto-grants-1997_02 |