Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Persulfate | HCID 62655 | — |
| Reactant | Benzonitrile, 3-(aminomethyl)- | HCID 457594 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | HCID 178527103 | HCID 178527103 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Cyanobenzoic acid | HCID 15875 | 56% |
Reaction Steps
A mixture containing m-cyanobenzylamine (13.2 g), acetonitrile (80 g), sodium hydrogencarbonate (76 g), water (500 g), sodium persulfate (95 g), and ruthenium oxide (0.25 g) was stirred for reaction at 80° C. over ten hours. After the precipitated solid was removed through filtration, the pH of the filtrate was adjusted to four through addition of sulfuric acid. The precipitated crystals were collected through filtration, washed with water, and dried, to thereby obtain 8.2 g of m-cyanobenzoic acid (yield 56%, based on m-cyanobenzylamine). The m-cyanobenzoic acid obtained had a purity of 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06433211B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-9f7afe34d1ad4429ba31b3470bf4778c |
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| Source note | uspto-grants-2002_08 |
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