反応式
[O-]CC.[Na+].[CH3:5][C:6]([CH3:16])=[CH:7][C@H:8]1[C:10]([CH3:12])([CH3:11])[C@H:9]1[C:13]([OH:15])=[O:14]>>[CH3:5][C:6]([CH3:16])=[CH:7][C@H:8]1[C:10]([CH3:11])([CH3:12])[C@@H:9]1[C:13]([OH:15])=[O:14]参加物
3
実験手順
As in Example 1, n-butyl cis-chryanthemate (25.0 g) was treated with sodium ethoxide (2.0 g) at 150°C for 60 minutes while stirring. By gas chromatographic analysis, the product was confirmed to be a mixture of the cis-isomer and the trans-isomer in a weight ratio of 25 : 75. The product was hydrolyzed by a conventional procedure and cis-chrysanthemic acid was removed as dihydro-chrysanthemolactone to give trans-chrysanthemic acid (15.1 g).
後処理
- additiona mixture of the cis-isomer
- customwas removed as dihydro-chrysanthemolactone
出典と根拠
- ORDレコード
- ord-f0adb64699734c49a4292328cfacb153
- 出典データセット
- uspto-grants-1976_01
- 特許番号
- US03931280
関連ノート
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