Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | 2-Butoxyethanol | HCID 8133 | — |
| Reactant | 2-Chloro-4,6-dimethylpyridine-3-carboxylic acid | HCID 591127 | — |
| Product | HCID 20393022 | HCID 20393022 | — |
Reaction Steps
A mixture consisting of 9.3 gm of 2-chloro-4,6-dimethyl-nicotinic acid, 5.41 gm of o-phenylenediamine and 25 ml of butyl glycol was heated at 170° C. for 90 minutes while stirring. The mixture was subsequently cooled to 60° C. and poured over ice. After adjusting it to a pH-value of 8 with ammonia, the mixture was suction-filtered, and the filter cake was washed with water and recrystallized from aqueous 70% acetic acid, yielding 53% of theory of the compound named in the heading, which had a melting point of 297°-299° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04167570 |
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| Source dataset | uspto-grants-1979_09 |
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| ORD ID | ord-d9a13c7b640c4772a7494681b669d569 |
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| Source note | uspto-grants-1979_09 |
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