Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Cyanopyridine | HCID 79 | — |
| Reactant | N,N-Dimethylbenzamide | HCID 11916 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Nicotinamide | HCID 936 | — |
| Product | Nicotinic Acid | HCID 938 | — |
Reaction Steps
To a 15-mL polypropylene centrifuge tube was added 3.73 mL of 50 mM potassium phosphate buffer (pH 7.0), 1.0 mL of a suspension of 22.1 mg dry cell weight E. coli SW132 wet cells (prepared as described in Example 10) in 50 mM potassium phosphate buffer (pH 7.0), and 0.2660 g of 3-cyanopyridine. The final concentration of 3-cyanopyridine was 0.501 M. The reaction mixture was mixed on a rotating platform at 23° C. After 15 minutes, 7.50 mL of 95:5 acetonitrile/water containing 0.30 M N,N-dimethylbenzamide (HPLC external standard) was added to the reaction, the resulting mixture centrifuged, and a 0.100 mL of the supernatant mixed with 0.900 mL of acetonitrile and analyzed by HPLC. The conversion of 3-cyanopyridine was 100%, and the yields of nicotinamide and nicotinic acid were 100% and 0%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07405064B2 |
|---|
| Source dataset | uspto-grants-2008_07 |
|---|
| ORD ID | ord-7ffd20477d814bb8af21b96958928593 |
|---|
| Source note | uspto-grants-2008_07 |
|---|