反応式
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([F:11])[C:3]=1[C:4](Cl)=[O:5].[F:12][C:13]([F:23])([F:22])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[NH:20][NH2:21].O>N1C=CC=CC=1>[F:12][C:13]([F:22])([F:23])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[N:20]([C:4](=[O:5])[C:3]1[C:7]([F:11])=[CH:8][CH:9]=[CH:10][C:2]=1[Cl:1])[NH2:21]参加物
実験手順
71.7 g (0.37 mol) of 2-chloro-6-fluorobenzoyl chloride are slowly added dropwise to a solution, cooled to 5° C., of 65.4 g (0.37 mol) of o-trifluoromethylphenylhydrazine in 200 ml of pyridine in such a manner that the temperature of the reaction mixture does not exceed 5° C. The mixture is stirred at room temperature for a further 90 minutes and subsequently treated with 400 ml of water. The aqueous phase is extracted three times with 150 ml of diethyl ether each time and the combined organic phases are washed in sequence with 2N sodium hydroxide solution and concentrated sodium chloride solution. The organic phase is then dried over anhydrous sodium sulfate and evaporated under reduced pressure, the crude product being evaporated twice with a small amount of toluene in order to remove excess pyridine. After recrystallization from methylene chloride/n-hexane there is obtained N1 -(α,α,α-trifluoro-o-tolyl)-2-chloro-6-fluorobenzhydrazide, m.p. 147°-148° C.; mass spectrum: 332(19), 157(100).
後処理
- customdoes not exceed 5° C
- extractionThe aqueous phase is extracted three times with 150 ml of diethyl ether each time
- washthe combined organic phases are washed in sequence with 2N sodium hydroxide solution and concentrated sodium chloride solution
- dry with materialThe organic phase is then dried over anhydrous sodium sulfate
- customevaporated under reduced pressure
- customthe crude product being evaporated twice with a small amount of toluene in order
- customto remove excess pyridine
- customAfter recrystallization from methylene chloride/n-hexane there
出典と根拠
- ORDレコード
- ord-8cd88cfd24194cfb877021c8cce7f585
- 出典データセット
- uspto-grants-1989_10
- 特許番号
- US04871757
関連ノート
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