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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750439Generated: October 31, 2026

3-Cyanopyridine → Nicotinamide

https://huagongshe.com/reaction/750439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-CyanopyridineHCID 79—
ReactantN,N-DimethylbenzamideHCID 11916—
ReactantAcetonitrile--water (1/1)HCID 18373917—
SolventAcetonitrileHCID 6342—
ProductNicotinamideHCID 936—
ProductNicotinic AcidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405064B2
Source datasetuspto-grants-2008_07
ORD IDord-5a630ca4120b4d7fa4ed3183819dbf17
Source noteuspto-grants-2008_07