Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 22370556 | HCID 22370556 | — |
| Solvent | Quinoline | HCID 7047 | — |
| Product | HCID 22370562 | HCID 22370562 | 70% |
Reaction Steps
In 5 ml of quinoline was dissolved 0.1 g of the 2-(4-carboxyphenyl)-6-methyl-4-quinolinecarboxylic acid obtained in Example 16 and solution was heated at 170° C. for 0.5 hour. Then the reaction mixture was poured into water, made alkaline by adding sodium carbonate and washed with toluene. The aqueous layer was neutralized with 3M hydrochloric acid until a precipitate was formed. After extracting with dichloromethane, 0.06 g of 4-(6-methylquinolin-2-yl)benzoic acid were obtained. NMR (270 MHz, CD3OD): δ 7.5-8.3 (m,9H); 2.56 (s,3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05780634 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-e861e15970084e7d881e26f28be8bd46 |
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| Source note | uspto-grants-1998_07 |
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