Nitric Acid → 1-(2-Fluoro-4-chloro-5-methylsulfonyloxyphenyl)-3,5-dimethyl-4-nitropyrazole
反応式
[F:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([O:9][S:10]([CH3:13])(=[O:12])=[O:11])=[CH:4][C:3]=1[N:14]1[C:18]([CH3:19])=[CH:17][C:16]([CH3:20])=[N:15]1.S(=O)(=O)(O)O.[N+:26]([O-])([OH:28])=[O:27]>O>[F:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([O:9][S:10]([CH3:13])(=[O:12])=[O:11])=[CH:4][C:3]=1[N:14]1[C:18]([CH3:19])=[C:17]([N+:26]([O-:28])=[O:27])[C:16]([CH3:20])=[N:15]1参加物
実験手順
To 1-(2-fluoro-4-chloro-5-methylsulfonyloxyphenyl)-3,5-dimethylpyrazole (31.9 g) was added 95% sulfuric acid (35 ml) and then added dropwise an acid mixture of 95% sulfuric acid (7.5 ml) and 61% nitric acid (10.3 g) under cooling with iced water, and the reaction mixture was stirred at room temperature for further one hour, and was then poured into iced water. The reaction mixture was extracted with toluene and the resulting toluene layer was washed with 1N aqueous sodium hydroxide solution and then with water and dried over anhydrous sodium sulfate. Removal of the solvent from.the extract in toluene by distillation in vacuo gave the titled compound (33.1 g) as a yellowish brown crystalline solid. Recrystallization of the solid from a mixture of cyclohexane/acetone yielded a pale yellow crystalline solid. m.p. 150.5°-152.5° C.
後処理
- additionadded dropwise
- extractionThe reaction mixture was extracted with toluene
- washthe resulting toluene layer was washed with 1N aqueous sodium hydroxide solution
- dry with materialwith water and dried over anhydrous sodium sulfate
- customRemoval of the solvent
- extractionfrom.the extract in toluene by distillation in vacuo
出典と根拠
- ORDレコード
- ord-2d1ecbbb4e1f459e8f83156527947ed3
- 出典データセット
- uspto-grants-1988_06
- 特許番号
- US04752326
反応ノート
読み込み中…