HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12390938, compound → 2-Cyclohexylamino-1,5,6-trihydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12390938 | HCID 12390938 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Cyclohexylamino-1,5,6-trihydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide | HCID 12390991 | — |
Reaction Steps
Using 1.91 parts of 5 % palladium-on-carbon, 1.89 parts of 2-cyclohexylamino-5,6-dihydroxy-3,4-dihydro-1(2H)-naphthalenone hydrobromide in 50 volume parts of water is subjected to catalytic reduction at ordinary temperature and pressure. When a stoichiometric amount of hydrogen has been absorbed, the reaction mixture is filtered to remove the catalyst and the filtrate is freeze-dried. The residue is recrystallized from a mixture of ethanol and ethyl acetate, whereby 2-cyclohexylamino-1,5,6-trihydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide is obtained as colorless crystals. Yield 1.38 parts; melting point: 230°-236° C (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04010202 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-f3edbb1fb9be4b6eb049f5b8fe126452 |
| Source note | uspto-grants-1977_03 |