GB869505A - Process for the preparation of cyclic di-and tri-carboxylic acids - Google Patents
Process for the preparation of cyclic di-and tri-carboxylic acidsInfo
- Publication number
- GB869505A GB869505A GB7789/59A GB778959A GB869505A GB 869505 A GB869505 A GB 869505A GB 7789/59 A GB7789/59 A GB 7789/59A GB 778959 A GB778959 A GB 778959A GB 869505 A GB869505 A GB 869505A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aromatic
- carboxylic acids
- water
- acid
- naphthalene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/803—Processes of preparation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process for the preparation of aromatic or aromatic-heterocyclic di- and tri-carboxylic acids or their alkali metal salts comprises reacting an aromatic hydrocarbon or heteroaryl compound free from carboxyl or other functional groups with alkali metal salts of aromatic or aromatic-heterocyclic carboxylic acids other than terephthalic acid (a) at a temperature of over 300 DEG C. under pressure, (b) in the absence of appreciable amounts of oxygen and water, (c) in the presence of substances which bind water or are capable of reacting with water, (d) in the presence of a protective gas (e) in the presence of cadmium, zinc, mercury or compounds thereof, and thereafter if desired, converting the alkali metal salts into the free acids. The carboxylic reactant is preferably the potassium salt of a mono-, di- or poly-carboxylic acid of the benzene series (other than salts of terephthalic acid) or of other aromatic series such as naphthalene, diphenyl and pyridine. The second reactant may be for example, benzene, naphthalene, diphenyl, pyridine, quinoline, isoquinoline, thiophene, thionaphthene or a ,a 1dipyridyl. The reaction may be carried out by heating in an atmosphere of carbon dioxide or nitrogen, preferably using cadmium fluoride as catalyst, and as water binding agent metal carbides, nitriles, borides or cyanates or elemental silicon or boron. Examples describe the preparation of terephthalic acid either alone or together with isocinchomeronic acid or pyridine di- and tri-carboxylic acids, and naphthalene 2,6-dicarboxylic acid. Specifications 828,028 and 847,246 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE869505X | 1958-03-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB869505A true GB869505A (en) | 1961-05-31 |
Family
ID=6802962
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7789/59A Expired GB869505A (en) | 1958-03-07 | 1959-03-06 | Process for the preparation of cyclic di-and tri-carboxylic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB869505A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0359098A1 (en) * | 1988-09-05 | 1990-03-21 | Nkk Corporation | Method of manufacturing alkali metal salt of 2,3,6,7-naphthalenetetracarboxylic acid |
-
1959
- 1959-03-06 GB GB7789/59A patent/GB869505A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0359098A1 (en) * | 1988-09-05 | 1990-03-21 | Nkk Corporation | Method of manufacturing alkali metal salt of 2,3,6,7-naphthalenetetracarboxylic acid |
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