反応式
[C:1]1([CH:7]=[N+]=[N-])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H][H].[CH:12](=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>ClCCl.C([O-])(=O)C.[Rh+2].C([O-])(=O)C>[C:1]1([CH:7]2[O:19][CH:12]2[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
6
実験手順
Phenyl diazomethane (1 mmol in 6 ml of t-butylmethylether) was added to a stirred solution of a sulphide of formula (B) wherein R' is hydrogen (0.2 mmol), rhodium (II) acetate (4.0 mg, 0.01 mmol) and benzaldehyde (1 mmol) in dichloromethane (4 ml) at room temperature over a period of 24 hours. After the addition was complete the solvent was removed in vacuo and the residue was chromatographed over silica [eluent dichloromethane:petrol (2:3)] to give the titled compound in 58% yield and 11% ee.
後処理
- customat room temperature
- customof 24 hours
- additionAfter the addition
- customwas removed in vacuo
- customthe residue was chromatographed over silica [eluent dichloromethane:petrol (2:3)]
出典と根拠
- ORDレコード
- ord-7c80eec67a9c44569f07a42c0ae4603b
- 出典データセット
- uspto-grants-1997_12
- 特許番号
- US05703246
関連ノート
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