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AssigneeHoechst Aktiengesellschaft
InventorsWilfried Bachmann, Christian Gnabs, Kurt Janecka, Eberhard Mundlos, Theodor Papenfuhs, Gerhard Waese
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An improved process for isolating 2-hydroxynaphthalenecarboxylic acids from reaction mixtures of the alkali metal salts of the 2-hydroxynaphthalene with carbon dioxide had been found which comprises diluting with water the reaction mixture which contains the di-alkali metal salt of 2-hydroxynaphthalenecarboxylic acid and 2-hydroxynaphthalene, while keeping the mixture at a temperature of at least 80.degree. C, then adjusting the pH-value to about 6 to 7 by means of aqueous mineral acid, separating the lower phase at at least 80.degree. C, cooling the upper phase to about 15.degree. to 25.degree. C, separating the 2-hydroxynaphthalene, then adjusting the pH-value to about 1 to 2 by means of aqueous mineral acid and isolating the separated 2-hydroxynaphthalenecarboxylic acid. By this novel process, work intensive operations, expensive technical apparatuses which are suspectible to repairs, solvents which do not participate directly in the reaction and therewith complicated regenerations, as known from the present art, are completely avoided. It permits clear and very easy separation of the reaction products at only one and the same stage in the process and allows in advantageous manner continuous operation.
A process for the isolation of 2-hydroxynaphthalenecarboxylic acid from its reaction mixture derived from the reaction of the alkali metal salts of 2-hydroxynaphthalene with carbon dioxide which comprises diluting the reaction mixture with such an amount of water that the ratio of water to organic product is about 4:1 to 6:1, maintaining the reaction mixture at a temperature of about 80.degree. to 100.degree. C, adjusting the pH to about 6 to 7 by addition of aqueous mineral acid, adding, if required, such an amount of 2-hydroxynaphthalene that 1 mole or more of 2-hydroxynaphthalene is present per mole of 2-hydroxynaphthalenecarboxylic acid, allowing the phases to separate into an upper and lower phase, separating the lower phase at a temperature of about 80.degree. to 100.degree. C, cooling said upper phase to a temperature of about 15.degree. to 25.degree. C to precipitate 2-hydroxynaphthalene, separating the precipitate, adjusting the pH of the remaining liquid upper phase to about 1 to 2 and isolating the 2-hydroxynaphthalenecarboxylic acid that has separated.
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