反応式
CN(C)C(=CC=[C:11]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:12]([O:14][CH2:15][CH3:16])=[O:13])C(OCC)=S.F[B-](F)(F)F.[CH3:29][N:30]([CH3:44])[C:31]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=O)=[CH:32][CH:33]=[N+](C)C.C([Li])CCC.C1([S:56]CC(OCC)=O)C=CC=CC=1>CCCCCC.O1CCCC1>[CH3:29][N:30]([CH3:44])[C:31](=[CH:32][CH:33]=[C:11]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[S:56]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
The procedure is as in Example 2 for the preparation of diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate, starting with N(3-dimethylamino-3-t-butyloxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (4.05 g), a 1.6M solution (8.8 cc) of butyllithium in hexane and ethyl (phenylthio)acetate (2.8 g) in tetrahydrofuran (65 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (70:30 by volume) as eluent, 6-ethyl 1-tert-butyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate (2.6 g), m.p. 85°-88° C., is obtained.
後処理
- customAfter purification by chromatography on a silica column
- additionwith a mixture of cyclohexane and ethyl acetate (70:30 by volume) as eluent
出典と根拠
- ORDレコード
- ord-c8c762a8393540459b15feb7cd32495a
- 出典データセット
- uspto-grants-1989_12
- 特許番号
- US04886835
関連ノート
読み込み中…