Nitric Acid → 1-(2-Fluoro-4-chloro-5-methylsulfonyloxyphenyl)-3,5-dimethyl-4-nitropyrazole
반응식
[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]1참가 물질
실험 절차
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.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-2d1ecbbb4e1f459e8f83156527947ed3
- 출처 데이터셋
- uspto-grants-1988_06
- 특허 번호
- US04752326
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