Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperonylamine | HCID 2723901 | — |
| Reactant | 3-Fluorophenylhydrazine hydrochloride | HCID 2723914 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 380002 | HCID 380002 | — |
Reaction Steps
4-Piperidone hydrochloride monohydrate (4.55 g) and 3-fluorophenylhydrazine hydrochloride (4.85 g) were added to ethanol (80 ml) and the mixture was heated under reflux for one hour. Hydrogen chloride gas was bubbled into the mixture and refluxing was recommenced for another 1.5 hours. The solution was cooled to 0° C., the hydrochloride was filtered off, washed with ethanol, dissolved in boiling water, decolourised with activated charcoal and filtered. 2M Sodium hydroxide solution was added to the warm solution until it was neutral when tested with pH paper. The pale cream solid was filtered off, washed with water and dried. Recrystallisation from acetonitrile gave a white solid which was a mixture of 7-fluoro and 9-fluoro-isomers in a ratio of 86:14 respectively (HPLC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05563147 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-58df874c4bff4fd2a6e4f8333825432c |
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| Source note | uspto-grants-1996_10 |
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