Benzophenone → Benzene, 1,1'-(1,6-heptadienylidene)bis-
反応式
C(C1C=CC=CC=1)(=O)C1C=CC=CC=1.[C:15]1([C:21]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[CH:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:15]1([C:21]([C:28]2[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=2)=[CH:22][CH2:23][CH2:24][CH2:25][CH:26]=[CH2:27])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1参加物
3
実験手順
In a reaction conducted in an analogous manner to Example 4, the reagent from Example 2 converted benzophenone into 1,1-diphenyl-1-heptene in a 71% yield. This product could easily be separated from reduction products by column chromatography on silica gel using hexane as the eluent, or even by simple distillation. This hydrocarbon was identified by spectral comparison with an authentic sample that was obtained by the partial reduction of known 1,1-diphenyl-1,6-heptadiene (J. J. Eisch et al., J. Am. Chem. Soc., 1979, 101: 1148).
後処理
- customThis product could easily be separated from reduction products by column chromatography on silica gel
- distillationeven by simple distillation
出典と根拠
- ORDレコード
- ord-c56f279c4b754bc0811128ed05757f25
- 出典データセット
- uspto-grants-1988_11
- 特許番号
- US04788368
反応ノート
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