6-fluoro-4-oxo-4H-chromene-2-carboxylic acid → 6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid

反応式

[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:9]([C:11]([OH:13])=[O:12])=[CH:8][C:7](=O)[C:6]=2[CH:15]=1.[H][H]>[Pd].C(O)(=O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH:9]([C:11]([OH:13])=[O:12])[CH2:8][CH2:7][C:6]=2[CH:15]=1

参加物

実験手順

A mixture of 63.4 parts of 6-fluoro-4-oxo-4H-1-benzopyran-2-carboxylic acid and 400 parts of acetic acid was hydrogenated at normal pressure and at room temperature with 3 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was stirred in petroleum ether. The product was filtered off and dried in vacuo at about 70° C., yielding 49 parts (83.3%) of 6-fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid (intermediate 5).