反応式
CN(C)C(=CC=C(C1C=CC=CC=1)C(OCC)=O)C(OCC)=S.F[B-](F)(F)F.[CH3:29][N:30]([CH3:42])[C:31]([C:37]([O:39][CH2:40][CH3:41])=[O:38])=[CH:32][CH:33]=[N+](C)C.CC[O-].[Na+].[CH:47]([C:50]1[CH:63]=[CH:62][C:53]([CH2:54][S:55][CH2:56][C:57]([O:59][CH2:60][CH3:61])=[O:58])=[CH:52][CH:51]=1)([CH3:49])[CH3:48]>C(O)C>[CH3:29][N:30]([CH3:42])[C:31](=[CH:32][CH:33]=[C:56]([S:55][CH2:54][C:53]1[CH:62]=[CH:63][C:50]([CH:47]([CH3:48])[CH3:49])=[CH:51][CH:52]=1)[C:57]([O:59][CH2:60][CH3:61])=[O:58])[C:37]([O:39][CH2:40][CH3:41])=[O:38]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
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-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (10 g), a 2M ethanolic solution of sodium ethylate (21 cc) and ethyl (4-isopropylbenzylthio)acetate (8.8 g) in ethanol (100 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (80:20 by volume) as eluent, diethyl 2-dimethylamino-5-(4-isopropylbenzylthio)-2,4-hexadienedioate (8.8 g) is obtained in the form of an orange-coloured oil, and is used in the crude state in the subsequent syntheses.
後処理
- customAfter purification by chromatography on a silica column
- additionwith a mixture of cyclohexane and ethyl acetate (80:20 by volume) as eluent
出典と根拠
- ORDレコード
- ord-c9742b85e75c4a6cb8887fefae125163
- 出典データセット
- uspto-grants-1990_11
- 特許番号
- US04971979
関連ノート
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