HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclobutanone → HCID 20316893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | HCID 12353616 | HCID 12353616 | — |
| Product | HCID 20316893 | HCID 20316893 | — |
| Product | HCID 20316906 | HCID 20316906 | — |
Reaction Steps
In a manner similar to that of Example 23, 1 part of 2-amino-5,6-dihydroxy-3,4-dihydro-1(2H)-naphthalenone hydrobromide is reacted with 20 volume parts of cyclobutanone. Via 2-cyclobutylideneamino-5,6-dihydroxy-3,4-dihydro-1(2H)-naphthalenone, 0.5 part of 2-cyclobutylamino-1,5,6-trihydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide is obtained as colorless crystals melting at 190°-200° C (decomposition). This product was identified as the compound according to Example 35 by mixed melting point.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04010202 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-46c931d8f59e4910916b39b96fda4ad1 |
| Source note | uspto-grants-1977_03 |