반응식
[Br:1][C:2]1[CH:8]=[CH:7][C:5](N)=[C:4]([C:9]2[CH2:13][CH2:12][O:11][N:10]=2)[C:3]=1[CH3:14].[ClH:15].N([O-])=O.[Na+].[S:20](=[O:22])=[O:21]>C(O)(=O)C.O.[Cu](Cl)Cl>[Br:1][C:2]1[CH:8]=[CH:7][C:5]([S:20]([Cl:15])(=[O:22])=[O:21])=[C:4]([C:9]2[CH2:13][CH2:12][O:11][N:10]=2)[C:3]=1[CH3:14]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 5 °C
실험 절차
At 15° C., a solution of 9 g (35 mmol) of 4-bromo-2-(4,5-dihydroisoxazol-3-yl)-3-methylaniline in 50 ml of glacial acetic acid is added to 15 ml of conc. hydrochloric acid. At 5-10° C., a solution of 2.44 g (35 mmol) of sodium nitrite in 10 ml of water is then added dropwise, and the mixture is stirred at 5° C. for 1 hour. At room temperature, this solution is then added dropwise to a mixture of a solution of 47 g (0.74 mol) of sulfur dioxide in 100 ml of glacial acetic acid and a solution of 2.23 g (13 mmol) of copper(II) chloride in 5 ml of water. The reaction mixture is stirred at room temperature for 1 hour and subsequently poured into 300 ml of ice-water and extracted with methylene chloride. The organic phase is washed with water, dried with magnesium sulfate and concentrated.
후처리
- stirringThe reaction mixture is stirred at room temperature for 1 hour
- extractionextracted with methylene chloride
- washThe organic phase is washed with water
- dry with materialdried with magnesium sulfate
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-ca4ace3ab43043a2a08b5f0069a97f16
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06706886B2
연결된 노트
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