反応式
[CH3:1][C:2](=C)[CH2:3][CH2:4]O.CC(C)=CC=O.CCCC.[C:17]1(=[O:23])[O:22][C:20](=[O:21])[CH:19]=[CH:18]1>>[C:20]1(=[O:21])[O:22][C:17](=[O:23])[C:18]2=[CH:1][CH:2]=[CH:3][CH:4]=[C:19]12参加物
5
実験手順
Examples of reactions which can be carried out particularly expediently in the reactors according to the invention are, without this listing being exhaustive: dehydrogenations, for example, of cyclohexylidene-aniline to give diphenylamine and of cyclohexenyl-cyclohexanone to give o-phenylphenol; hydrogenations, for example, of nitrobenzene to give aniline and of phenol to give cyclohexanone; oxidative alcohol dehydrogenations, for example, of 3-methyl-3-buten-1-ol to give 3-methyl-2-buten-1-al; selective oxidations of hydrocarbons, for example, of n-butane to give maleic anhydride, of oxylene to give phthalic anhydride and of propene to give acrolein or acrylic acid and alkylations and halogenations.
出典と根拠
- ORDレコード
- ord-d20fddd0836f4a3da7beff7e8dc9062b
- 出典データセット
- uspto-grants-1996_01
- 特許番号
- US05484576
関連ノート
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