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ChemicalBook CAS DataBase List 4-Formyl-4'-methyl-2,2'-bipyridine
104704-09-8

4-Formyl-4'-methyl-2,2'-bipyridine synthesis

6synthesis methods
-

Yield: 49.1%

Reaction Conditions:

Stage #1:4-methyl-2,2'-bipyridine with selenium(IV) oxide in 1,4-dioxane for 24 h;Reflux;Inert atmosphere;
Stage #2:ethyl acetate for 1 h;Reflux;

Steps:


EXAMPLE. 4’-methyl-2,2’-bipyridine-4-carbaldehyde. The synthesis of 4’-methyl-2,2’-bipyridine-4-carbaldehydewas performed from a previously procedure (Peek et al., Int J Pept Protein Res, 38.2: 114-23 (1991)). In a 200 mLround-bottomed flask was 4’-methyl-2,2’-bipyridine (1.5 g, 8.14 mmol) in Dioxane (62.6 ml). Argon was bubble into thesolution for 15 minutes before the addition of selenium dioxide (1.012 g, 9.12 mmol). Argon was bubbled for another 20minutes before heating the solution at reflux for 24 hrs. After the flask was cooled to room temperature the solution wasfiltered and the solvent reduced. The remaining solid was dissolved in ethyl acetate and heated at reflux for 1 hr followedby a hot filtration. The filtrate was then washed with 0.1 M sodium carbonate and extracted with 0.3 M sodium metabisulfate.The pH of the aqueous layer was adjusted to 10 with sodium bicarbonate and the product was extracted withDCM. The solvent was removed under vacuum and no further purification was need for the white solid. (Yield: 49.1 %).

References:

Purdue Research Foundation;CHMIELEWSKI, Jean, A.;PIRES, Marcos, M.;PRZYBYLA, David, E. EP2300033, 2016, B1 Location in patent:Paragraph 0120

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