Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-Methylpyridine | HCID 7970 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Catalyst | Manganous Acetate | HCID 12525 | — |
| Catalyst | Tetrapropylammonium bromide | HCID 74745 | — |
| Solvent | Water | HCID 962 | — |
| Product | Nicotinic Acid | HCID 938 | — |
Reaction Steps
The same autoclave as that used in Example 1 was charged with 25 parts by weight of 3-methylpyridine, 0.38 part by weight of cobalt acetate, 0.27 part by weight of manganese acetate, 1 part by weight of tetrapropylammonium bromide and 150 parts by weight of acetic acid having a 5 wt % water content, and the mixture was allowed to react in the same manner as in Example 1 to give 21.7 parts by weight of a crude nicotinic acid crystal. The conversion of the 3-methylpyridine was 93.7 mol %, the selectivity to the nicotinic acid was 99.0 mol %, and the yield of the nicotinic acid 92.8 mol %. The conversion and the yield in Example 2 were improved over those in Example 1 since the solvent was used in a larger amount in Example 2. The crude nicotinic acid had a bromine concentration of 608 ppm and showed a dissolved b value of 5.44.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05700944 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-564dcfae0a3f459a83c031a0c2306f9a |
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| Source note | uspto-grants-1997_12 |
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