Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Benzilic acid | HCID 6463 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20380322 | HCID 20380322 | 10.4% |
Reaction Steps
A mixture of 11.4 grams (0.05 mole) of benzilic acid and 4.7 grams (0.05 mole) of 4-aminopyridine was heated at 220° C. for 3.5 hours. After cooling the mixture was dissolved in toluene and washed with 10% sodium carbonate solution and with 2 N hydrochloric acid. The acidic extracts were basified with 5 N sodium hydroxide and the resulting oil extracted into toluene. After drying over magnesium sulphate, the toluene was removed and the yellow oil was recrystallised from light petroleum (b.p. 80°-100° C.) giving 1.35 grams (10% yield) of the title compound, m.p. 152° to 154° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04180670 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-8437ab2591bc465faf0701f23e42172f |
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| Source note | uspto-grants-1979_12 |
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