Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21437921 | HCID 21437921 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | HCID 21437928 | HCID 21437928 | — |
Reaction Steps
A mixture of 6.6 gm (0.018 mol) of ethyl 4-(2'-bromo-4-biphenylyl)-4-oxo-butyrate (m.p. 61°-62° C.), 3 gm of 100% hydrazine hydrate and 100 ml of diethyleneglycol was heated at 100° C. for 20 minutes. Then, 5 gm of pulverized potassium hydroxide were added. After refluxing for 5 hours, the reaction mixture was poured into 500 ml of water, acidified with dilute hydrochloric acid, and the precipitate was dissolved in ether. The ether solution was washed with water, dried and evaporated; the residue was dissolved in acetone, and by addition of cyclohexylamine the cyclohexylamine salt of 4-(2'-bromo-4-biphenylyl)-butyric acid, m.p. 148°-149° C. (from acetone), was obtained. Melting point of the free acid: 63° C. (from cyclohexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04021479 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-6e55bd921be04d2a809c8c8057e40391 |
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| Source note | uspto-grants-1977_05 |
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