Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 14555665 | HCID 14555665 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | HCID 14555668 | HCID 14555668 | 60.4% |
Reaction Steps
To a solution of 3.4 gms KOH in 23 ml diethylene glycol was added 5.4 gms 9(4-chlorophenyl)-7-ketononanoic acid and 3 ml hydrazine hydrate. The resulting mixture was heated at 145° for 1 hour. The mixture was cooled, attached to a water aspirator, and the excess water and hydrazine distilled off. The mixture was then re-heated to 145° for 3 hours and cooled. The oily reaction mixture was diluted with water, acidified with conc. HCl, and the precipitated solid filtered off. Since the NMR showed starting material still present, the solid was dissolved in 25 ml diethylene glycol and 4.1 ml hydrazine hydrate was added. This solution was refluxed for 3 hr, then the water and hydrazine were distilled off under vacuum as before. 5.2 gms KOH was added and the resulting mixture was heated at 160° for 3.5 hours, then cooled to room temperature overnight. It was dissolved in water and acidified with conc. HCl. The precipitated solid was dissolved in 10% KOH solution, washed three times with ether, filtered, acidified with conc. HCl, and placed in the cold overnight. The solid was filtered off, dried and recrystallized from hexanes to give 3.1 gm white solid of m.p. 73°-5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04861798 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-5a488cea0ea64d0fae406a29a1aa8cae |
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| Source note | uspto-grants-1989_08 |
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