Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118411Generated: October 25, 2026

Potassium Carbonate → 4-Ethyl-2-methylpyridine

https://huagongshe.com/reaction/2118411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DimethylpyrazineHCID 22201—
Reactant2,3-Dihydro-5,6-dimethylpyrazineHCID 85225—
ReactantPyridine, 2-methyl-4-nitro-, 1-oxideHCID 95291—
Product4-Ethyl-2-methylpyridineHCID 68307—
Product4-Methoxy-2-methylpyridineHCID 4737758—
Product2-Methyl-4-methoxypyridine-N-oxideHCID 10701893—

Reaction Steps

In the examples, certain of the starting materials were prepared in accordance with methods disclosed in the literature. For example, 2,3-dimethylpyrazine was prepared from 2,3-dimethyl-5,6-dihydropyrazine by the method of G. P. Rizzi, J. Org. Chem. 33, 1333 (1968) which itself was prepared by the procedure of T. Ishiguro and M. Matsumura, Yak. Zass. 78, 229 (1958). 4-Ethyl-2-methylpyridine was prepared by the procedure of Kaiser et al., J. Org. Chem. 38, 71 (1973). 4-Methoxy-2-picoline-N-oxide was prepared by reacting 4-nitro-2-picoline-N-oxide with methanolic potassium carbonate solution according to the general procedure of E. Profft et al., Germany (East) 69, 126; 10/5/69; Chem. Abs. 72, 90309w (1970). The crude product was not purified but was reacted directly with phosphorous trichloride in chloroform solution to give the known 4-methoxy-2-picoline starting material, based upon the general method of Herz and Tsai, J. Am. Chem. Soc. 76, 4184 (1954).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04678501
Source datasetuspto-grants-1987_07
ORD IDord-fac269ef987e4cdea9a50d4deedd9982
Source noteuspto-grants-1987_07