Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl 4-oxocyclohexanecarboxylate | HCID 317638 | — |
| Reactant | (4-(Benzyloxy)phenyl)hydrazine monohydrochloride | HCID 3016725 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19710734 | HCID 19710734 | 83% |
Reaction Steps
To a suspension of 3.242 gm (12.93 mMol) 4-benzyloxy-phenylhydrazine hydrochloride in 80 mL ethanol were added 1.05 mL (12.93 mMol) pyridine. The resulting mixture was heated to 50° C. for about 20 minutes and then 1.87 mL (11.75 mMol) ethyl 4-oxocyclohexanecarboxylate were added. The resulting mixture was stirred at reflux for 18 hours. The reaction mixture was then concentrated under reduced pressure and the residue partitioned between water and ethyl acetate. The organic phase was separated, washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 35% ethyl acetate in hexane. Fractions containing product were combined and concentrated under reduced pressure to give 3.38 gm (83%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380201B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-33d314bce17c4c5783618cf8c17a543a |
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| Source note | uspto-grants-2002_04 |
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