Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Ethyl 3-oxo-5-phenylpentanoate | HCID 61162 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66777263 | HCID 66777263 | 84% |
Reaction Steps
A mixture of ethyl 3-oxo-5-phenylpentanoate (5.8 g) and dimethylformamide dimethylacetal (3.6 mL) was stirred at 100° C. overnight, and the mixture was allowed to cool to room temperature. To the reaction mixture were added ethanol (30 mL) and phenylhydrazine (2.9 g), and the mixture was further stirred at 100° C. for 8 hr. After allowing to cool, ethanol was evaporated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:10, volume ratio) to give the title object compound (7.1 g, 84%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436043B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-80f9d97bf55249ad856d489c50721e81 |
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| Source note | uspto-grants-2013_05 |
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