Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-Chloropyridine-2-carbonyl chloride--hydrogen chloride (1/1) | HCID 22397270 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Picolinic acid | HCID 1018 | — |
Reaction Steps
A reaction vessel is laden with methylamine as a 40% aqueous solution (117 kg, 1507 mol of methylamine). Water (97.5 kg) is added and the solution is cooled to −5° C. A solution of the crude 4-chloropyridine-2-carbonyl chloride hydrochloride (approx. 330 kg, including toluene, obtained from 60 kg of 2-picolinic acid by the process detailed in stage 1/method 1a) in toluene is added to such a degree that the temperature of the reaction mixture does not exceed 30° C. After stirring further at 20° C. for 1 h, the insoluble constituents are filtered out of the reaction mixture. After the phases have been separated, the organic phase is washed with water (90 kg). For better phase separation, 5 kg of sodium chloride are added. The majority of the toluene is distilled out of the organic phase under reduced pressure (final vacuum 40 mbar at jacket temperature 95° C.). The crude 4-chloro-N-methylpyridine-2-carboxamide is thus obtained as an orange- to dark brown-colored oil and is used in the next stage without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124782B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-cff8e7acd8ee46d4b9321d6ddce967b6 |
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| Source note | uspto-grants-2012_02 |
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