HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20380271, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12669653 | HCID 12669653 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20380271 | HCID 20380271 | — |
Reaction Steps
A mixture of 1 part of 3,9-dihydro-3,9-dioxo-1-phenyl-2H-indeno[2,1-c]pyridine-4-carbonitrile, 5 parts of potassium hydroxide, and 39 parts of 1,1-dimethylethanol is heated at the boiling point under reflux for 16 hours. The resultant mixture is diluted with 1000 parts of water, followed by sufficient acetic acid to neutralize the base present. The precipitate which forms is filtered off; consecutively washed with water, methanol, and 1,1'-oxybisethane; and dried in vacuo. The resultant yellow solid is crystallized from aqueous N,N-dimethylformamide to afford 3,9-dihydro-1-phenyl-2H-indeno[2,1-c]pyridine-4-carboxamide melting above 300°. The product has the formula ##STR19##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04180666 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-bf0756fa7efc4945ac465a32c1fa6888 |
| Source note | uspto-grants-1979_12 |