HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21551659, compound → HCID 21551677, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21551659 | HCID 21551659 | — |
| Reactant | HCID 21551680 | HCID 21551680 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21551677 | HCID 21551677 | — |
Reaction Steps
20.6 g. (50 mMole) 1-[3-(5,6,7,8-tetrahydronaphth-1-yloxy)-2-hydroxy-prop-1-yl]-4-(2-nitrophenyl)-piperazine (prepared in the manner described in Example 9) were hydrogenated in tetrahydrofuran, in the presence of Raney nickel in a manner analogous to that described in Example 7. There were thus obtained 19.4 g. (85% of theory) 1-[3-(5,6,7,8-tetrahydronaphth-1-yloxy)-2-hydroxy-prop-1-yl]-4-(2-aminophenyl)-piperazine dihydrochloride, which has a melting point of 268°-271°C. The free base obtained herefrom in the usual manner melts at 103°-104°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947446 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-6a775326e93c4d9e9dda19c007a47768 |
| Source note | uspto-grants-1976_03 |