Salicylaldehyde → 3,4-Dihydro-3'-methyl-4-(3-methyl-2-benzothiazolinylidenemethyl)spiro[2H-1-benzopyran-2,2'-benzothiazoline]
反応式
[S:1]([C:5]1[CH:11]=[CH:10][C:8](C)=[CH:7][CH:6]=1)([O-])(=O)=O.[CH3:12][C:13]1[S:14][C:15]2[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=2[N+:17]=1[CH3:18].[CH:23]1[CH:28]=[C:27]([CH:29]=O)[C:26]([OH:31])=[CH:25][CH:24]=1.[NH:32]1[CH2:37]CC[CH2:34][CH2:33]1>C(O)C>[CH3:18][N:17]1[C:16]2[CH:19]=[CH:20][CH:21]=[CH:22][C:15]=2[S:14][C:13]21[CH2:12][CH:29]([CH:34]=[C:33]1[N:32]([CH3:37])[C:11]3[CH:10]=[CH:8][CH:7]=[CH:6][C:5]=3[S:1]1)[C:27]1[CH:28]=[CH:23][CH:24]=[CH:25][C:26]=1[O:31]2参加物
5
実験手順
40.2 g of 2,3-dimethylbenzothiazolium tosylate and 7.32 g of salicylic aldehyde were mixed in 1200 ml of ethanol; to this mixture were added 12 ml of piperidine with stirring. Stirring was continued for 1 hour at room temperature. A precipitate was formed which was filtered out and washed with ethanol.
後処理
- stirringStirring
- customA precipitate was formed which
- filtrationwas filtered out
- washwashed with ethanol
出典と根拠
- ORDレコード
- ord-d96a7052256b4491968160022c1a4b1a
- 出典データセット
- uspto-grants-1981_12
- 特許番号
- US04306017
反応ノート
読み込み中…