Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940889Generated: October 30, 2026

Acetic Acid → Nicotinic Acid

https://huagongshe.com/reaction/1940889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-MethylpyridineHCID 7970—
CatalystCobalt diacetateHCID 6277—
CatalystManganous AcetateHCID 12525—
CatalystTetrapropylammonium bromideHCID 74745—
SolventWaterHCID 962—
ProductNicotinic AcidHCID 938—

Reaction Steps

The same autoclave as that used in Example 1 was charged with 25 parts by weight of 3-methylpyridine, 0.38 part by weight of cobalt acetate, 0.27 part by weight of manganese acetate, 1 part by weight of tetrapropylammonium bromide and 150 parts by weight of acetic acid having a 5 wt % water content, and the mixture was allowed to react in the same manner as in Example 1 to give 21.7 parts by weight of a crude nicotinic acid crystal. The conversion of the 3-methylpyridine was 93.7 mol %, the selectivity to the nicotinic acid was 99.0 mol %, and the yield of the nicotinic acid 92.8 mol %. The conversion and the yield in Example 2 were improved over those in Example 1 since the solvent was used in a larger amount in Example 2. The crude nicotinic acid had a bromine concentration of 608 ppm and showed a dissolved b value of 5.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05700944
Source datasetuspto-grants-1997_12
ORD IDord-564dcfae0a3f459a83c031a0c2306f9a
Source noteuspto-grants-1997_12