Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Ethyl 2-oxocyclohexanecarboxylate | HCID 95543 | — |
| Product | HCID 16063552 | HCID 16063552 | — |
Reaction Steps
To a solution of cyclohexanone-2-carboxylic acid ethylester (0.6 g) in acetic acid (1 mL) in a round bottom flask under argon was added phenylhydrazine (0.38 g). The mixture was immersed into an oil bath and heated to 120° C. overnight. The reaction vessel was then cooled and the acetic acid was evaporated in vacuo and the remaining solid was dissolved in EtOAc and water. The phases were separated and the aqueous phase was extracted with further EtOAc. The combined organic phases were washed with brine, dried over sodium sulfate, filtered and evaporated in vacuo and azeotroped with toluene (2×). The crude residue was then purified via ISCO Combiflash chromatography (eluting with EtOAc/heptane) to afford the desired 2-phenyl-1,2,4,5,6,7-hexahydro-indazol-3-one (0.56 g) as a light brown solid. MS (ESI+): 215.4 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652057B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-e904886cc2164d16900bb6da0a188193 |
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| Source note | uspto-grants-2010_01 |
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