反応式
[CH3:1][C:2]1[C:3]2[C:8]([C:9]([CH3:16])=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2>[Cr]([O-])([O-])=O.[Cu+2].C1(C)C=CC=CC=1>[CH3:1][CH:2]1[C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=2[CH:9]([CH3:16])[C:10]2[C:15]1=[CH:14][CH:13]=[CH:12][CH:11]=2参加物
4
実験手順
9,10-Dihydro-9,10-dimethylanthracene was prepared by hydrogenation of 9,10-dimethylanthracene with Girdler G-22 copper chromite catalyst in toluene at 120° C. and 1500 psi for 1 hour. The mixtures resulting from five such runs were combined and filtered, and the off-white solid product was isolated by evaporating the solvent. It was characterized by nmr spectroscopy.
後処理
- customThe mixtures resulting from five such runs
- filtrationfiltered
- customthe off-white solid product was isolated
- customby evaporating the solvent
出典と根拠
- ORDレコード
- ord-33838fd7755847479484c70ff8d9c312
- 出典データセット
- uspto-grants-1978_12
- 特許番号
- US04131646
関連ノート
読み込み中…