Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Coumalic acid | HCID 68141 | — |
| Product | HCID 178418479 | HCID 178418479 | — |
Reaction Steps
2-Hydroxypyridine or quinoline carboxylic acids and esters are useful as herbicide and pharmaceutical intermediates. One method for their preparation involves oxidizing quinolinic acid to obtain 2 3-bis(methoxycarbonyl)pyridine N-oxide, treating the N-oxide with acetic anhydride to give the 2-acetoxy compound, and hydrolyzing to give 6-hydroxy-2,3-dimethoxycarboxylpyridine in 27.5% overall yield; see E. Spinner et al., J. Chem. Soc. (B), 289 (1971). Another method involves reacting an ester of coumalic acid with ammonia to yield 2-hydroxy-5-pyridinecarboxylic acid; see W. T. Caldwell et al. J. Am. Chem. Soc. 66, 1479 (1944). Another method involves converting alpha-pyrone-6-carboxylic acid with ammonium acetate and glacial acetic acid into 2-pyridine-6-carboxylic acid; see J. Fried et al., J. Org. Chem. 6, 566 (1941).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968803 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-776136bbcb8443b7b0c2b7e08aa6cb65 |
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| Source note | uspto-grants-1990_11 |
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