Chemical Research in 3194-15-8

From this literature《Two methods for conversion of an aromatic aldehyde to a 4-arylpyridine. A method for preparation of 3-alkyl-4-arylpyridines》,we know some information about this compound(3194-15-8)Application In Synthesis of 1-(Furan-2-yl)propan-1-one, but this is not all information, there are many literatures related to this compound(3194-15-8).

Carbateas, P. M.; Williams, Gordon L. published the article 《Two methods for conversion of an aromatic aldehyde to a 4-arylpyridine. A method for preparation of 3-alkyl-4-arylpyridines》. Keywords: pyridine nitrophenyl; methylpyridine nitrophenyl; nitrophenylpyridine.They researched the compound: 1-(Furan-2-yl)propan-1-one( cas:3194-15-8 ).Application In Synthesis of 1-(Furan-2-yl)propan-1-one. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:3194-15-8) here.

Reaction of 1-(2-furyl)-3-(m-nitrophenyl)propenone with 2-acetylfuran (I) and NH4OAc in AcOH at reflux gave 2,6-di(2-furyl)-4-(m-nitrophenyl)pyridine, which was oxidized with dilute HNO3 and the resultant 4-(m-nitrophenyl)-2,6-pyridinedicarboxylic acid decarboxylated by heating with Dowtherm to give 4-(m-nitrophenyl)pyridine (II). II was alternatively prepared by heating a mixture of m-O2NC6H4CHO, CHCCO2Me, and NH4OAc in AcOH at reflux, oxidizing the product (III) with dil HNO3, hydrolyzing the resultant di-Me 4-(m-nitrophenyl)-3,5-pyridinedicarboxylate, and decarboxylating the diacid. 3-Methyl-4-(m-nitrophenyl)pyridine was prepared by replacing I with 2-propionylfuran in the first synthesis.

From this literature《Two methods for conversion of an aromatic aldehyde to a 4-arylpyridine. A method for preparation of 3-alkyl-4-arylpyridines》,we know some information about this compound(3194-15-8)Application In Synthesis of 1-(Furan-2-yl)propan-1-one, but this is not all information, there are many literatures related to this compound(3194-15-8).

Reference:
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem