Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Cyanopyridine | HCID 79 | — |
| Reactant | N,N-Dimethylbenzamide | HCID 11916 | — |
| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Nicotinamide | HCID 936 | — |
| Product | Nicotinic Acid | HCID 938 | — |
Reaction Steps
At the completion of the reaction (100% conversion of nitrile), the product mixture was decanted from the biocatalyst beads, and 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture), 16.56 mL of distilled, deionized water, and 2.127 g of 3-cyanopyridine was added to the catalyst beads in the reaction vessel. The final concentration of 3-cyanopyridine was 1.06 M in 20 mL of reaction mixture. Samples (0.100 mL) of the reaction mixture were mixed with 0.400 mL of 95:5 acetonitrile/water containing 0.30 M N,N-dimethylbenzamide (HPLC external standard), and a 0.100 mL of the resulting solution mixed with 0.900 mL of acetonitrile and analyzed by HPLC. After 23 h, the conversion of 3-cyanopyridine was 100%, and the yields of nicotinamide and nicotinic acid were 100% and 0%, respectively. The initial reaction rate for production of nicotinamide, measured during the first 30 min of reaction, was 4.60 mM/minute.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153663B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-28ee249c146a407591ccd3f4ec516037 |
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| Source note | uspto-grants-2006_12 |
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