反応式
[C:1]1([C:7]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)([CH:11]2[CH2:16][CH2:15]C[N:13]([CH2:17][CH3:18])[CH2:12]2)C(N)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(C(C2C=CC=CC=2)(C2C=CN(CC)C=CC=2)C(N)=O)C=CC=CC=1>>[CH2:17]([N:13]1[CH2:15][CH2:16][C:11](=[C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH2:12]1)[CH3:18]参加物
3
実験手順
Following the same procedure, employing α,α-diphenyl-α-(1-ethyl-3-piperidinyl)acetamide or α,α-diphenyl-α-(1-ethyl-4-azepinyl)acetamide as the starting material yields 1-ethyl-3-diphenylmethylenepyrrolidine or 1-ethyl-4-diphenylmethyleneazepine, respectively.
出典と根拠
- ORDレコード
- ord-5753af85d8bd4345b11bead3a140e7d8
- 出典データセット
- uspto-grants-1980_12
- 特許番号
- US04242261
関連ノート
読み込み中…