3-(Trifluoromethyl)benzaldehyde → 3-[(1,3-Benzodithiol-2-ylidene)amino]-2-thioxo-5-[[3-(trifluoromethyl)phenyl]methylene]-4-thiazolidinone
反応式
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[S:3][C:2]1=[N:10][N:11]1[C:15](=[O:16])[CH2:14][S:13][C:12]1=[S:17].[F:18][C:19]([F:29])([F:28])[C:20]1[CH:21]=[C:22]([CH:25]=[CH:26][CH:27]=1)[CH:23]=O.C(O)(=O)C.N1CCCCC1>C(COC)OC.ClCCl>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[S:3][C:2]1=[N:10][N:11]1[C:15](=[O:16])[C:14](=[CH:23][C:22]2[CH:25]=[CH:26][CH:27]=[C:20]([C:19]([F:18])([F:28])[F:29])[CH:21]=2)[S:13][C:12]1=[S:17]参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
A slurry of 3-[(1,3-benzodithiol-2-ylidene)amino]-2 -thioxo-4-thiazolidinone (see example 37), m-trifluoromethylbenzaldehyde (10 ml, excess) and acetic acid/piperidine (1 ml) in 250 ml of anhydrous glyme is heated at reflux for seven days. The reaction mixture is concentrated in vacuo and the oily residue extracted with hexane. The solid thus obtained is slurried in 1000 ml of dichloromethane and stirred at room temperature overnight. The slurry is filtered and the filtrate concentrated in vacuo. The solid residue thus obtained is recrystallized from dimethylformamide to yield 500 mg of the title compound, melting point 268°-269° C.
後処理
- temperatureat reflux for seven days
- concentrationThe reaction mixture is concentrated in vacuo
- extractionthe oily residue extracted with hexane
- customThe solid thus obtained
- filtrationThe slurry is filtered
- concentrationthe filtrate concentrated in vacuo
- customThe solid residue thus obtained
- customis recrystallized from dimethylformamide
出典と根拠
- ORDレコード
- ord-352d71ab6e3e430ebddb6a92b9110eab
- 出典データセット
- uspto-grants-1978_08
- 特許番号
- US04107175
反応ノート
読み込み中…