反応式
Cl[C:2](=[CH2:5])[C:3]#[N:4].[Cl:6][C:7]1[CH:12]=[C:11]([C:13]([F:16])([F:15])[F:14])[CH:10]=[C:9]([Cl:17])[C:8]=1[NH:18][NH2:19].C(N(CC(O)=O)CC(O)=O)CN(CC([O-])=O)CC([O-])=O.[Na+].[Na+].S(=O)(=O)(O)O.C(=O)([O-])[O-].[Na+].[Na+]>CO>[NH2:4][C:3]1[N:18]([C:8]2[C:7]([Cl:6])=[CH:12][C:11]([C:13]([F:14])([F:16])[F:15])=[CH:10][C:9]=2[Cl:17])[N:19]=[CH:5][CH:2]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 1
実験手順
25 ml (27.6 g/0.3 mol) of 2-chloro-acrylonitrile are added dropwise to 24.5 g (0.1 mol) of 2,6-dichloro-4-trifluoromethylphenylhydrazine and 20 mg of disodium ethylenediamine-tetraacetate (Titriplex III) in 150 ml of methanol at the reflux temperature. When the addition has ended, the mixture is heated at the reflux temperature for a further 8 hours, 9 ml (0.16 mol) of 96% strength sulphuric acid are added dropwise and the mixture is heated at the reflux temperature for a further 6 hours. 33.5 g (0.3 mol) of anhydrous sodium carbonate are added to the cooled reaction mixture. After 4 hours, the solvent is removed in vacuo, the residue is taken up in 500 ml of water and the mixture is stirred at room temperature for 10 hours. The precipitate which has separated out is filtered off, rinsed with water and dried in vacuo at 50° C. 28.5 (96% of theory) of 5-amino- 1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole of melting point 103°-105° C. are obtained.
後処理
- additionWhen the addition
- temperaturethe mixture is heated at the reflux temperature for a further 8 hours
- temperaturethe mixture is heated at the reflux temperature for a further 6 hours
- customthe solvent is removed in vacuo
- customThe precipitate which has separated out
- filtrationis filtered off
- washrinsed with water
- customdried in vacuo at 50° C
出典と根拠
- ORDレコード
- ord-2f9c91db730d4cb688408c810237d2d2
- 出典データセット
- uspto-grants-1988_09
- 特許番号
- US04772309
関連ノート
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