反応式
[Cl:1]([O-:5])(=[O:4])(=[O:3])=[O:2].[CH2:6]([N:8]1[C:16](OC)=[C:15]2[C:10]([CH:11]=[CH:12][CH:13]=[CH:14]2)=[C:9]1[CH:19]=[CH:20][C:21]1[O:22][C:23]2[CH:31]=[CH:30][CH:29]=[CH:28][C:24]=2[N+:25]=1[CH2:26][CH3:27])[CH3:7].C1(C)C=CC(S([O-])(=O)=O)=CC=1.[CH2:43]([N+:45]1[C:49]2[CH:50]=[CH:51][CH:52]=[CH:53][C:48]=2[S:47][C:46]=1[CH3:54])[CH3:44].C(N(CC)CC)C>C(#N)C>[Cl:1]([O-:5])(=[O:4])(=[O:3])=[O:2].[CH2:6]([N:8]1[C:16]([CH:54]=[C:46]2[N:45]([CH2:43][CH3:44])[C:49]3[CH:50]=[CH:51][CH:52]=[CH:53][C:48]=3[S:47]2)=[C:15]2[C:10]([CH:11]=[CH:12][CH:13]=[CH:14]2)=[C:9]1[CH:19]=[CH:20][C:21]1[O:22][C:23]2[CH:31]=[CH:30][CH:29]=[CH:28][C:24]=2[N+:25]=1[CH2:26][CH3:27])[CH3:7]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
2-[2-(2-Ethyl-3-methoxyisoindol-1-yl)vinyl]-3-ethyl-benzoxazolium perchlorate (1.0 g) and 3-ethyl-2-methylbenzothiazolium p-toluenesulfonate (0.9 g) were dissolved in acetonitrile. Triethylamine was added and the reaction mixture stirred until the absorption at 520 nm disappeared. The reaction mixture was evaporated to dryness and chromatographed on silica gel. After recrystallization of the product from methanol, the melting point was 180° C. CH3CN λ max 625 nm.
後処理
- customThe reaction mixture was evaporated to dryness
- customchromatographed on silica gel
- customAfter recrystallization of the product from methanol
出典と根拠
- ORDレコード
- ord-abd11817a4754010927b1f70aef32e3c
- 出典データセット
- uspto-grants-1977_06
- 特許番号
- US04030932
関連ノート
読み込み中…