Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Glycerol | HCID 753 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Aminobenzoic Acid | HCID 7419 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 30904-40-6 | HCID 3906961 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Quinoline-5-carboxylic acid | HCID 232489 | 35.2% |
Reaction Steps
To a solution containing 15 g (0.1 mol) of m-aminobenzoic acid, 27 g (0.13 mol) of m-nitrobenzene sulfonate and 25 g (0.4 mol) of glycerol, was added 125 g of 70% sulfuric acid. The resultant reaction mixture was refluxed for about 2.5 hours, diluted with 125 mL of water, basified to pH 9 using ammonium hydroxide, stirred overnight with 5 g of charcoal, and then filtered. The filtrate was then boiled with 5 g charcoal, filtered, and then cooled to 50° C., acidified to pH 5 with glacial acetic acid (15 mL), and filtered to provide a brown solid. This solid was boiled in 300 mL of water containing 10 mL of acetic acid and hot filtered to provide crude material. This material was purified using recrystallization from boiling acetic acid to provide 6.1 g of a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05484926 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-300d65a4775141c18ecc4d72bc129d3f |
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| Source note | uspto-grants-1996_01 |
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