반응식
[CH3:1][N:2]([CH3:11])[S:3]([N:6]1[CH:10]=[CH:9][CH:8]=[N:7]1)(=[O:5])=[O:4].C([Li])CCC.[Cl:17]C(Cl)(Cl)C(Cl)(Cl)Cl>O1CCCC1.CCCCCC>[Cl:17][C:8]1[CH:9]=[CH:10][N:6]([S:3]([N:2]([CH3:11])[CH3:1])(=[O:4])=[O:5])[N:7]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
To a solution of N-dimethylsulfamoylpyrazole (188.0 g, 1.07 mol) in dry tetrahydrofuran (1500 mL) at −78° C. was added dropwise a solution of 2.5 M n-butyl-lithium (472 mL, 1.18 mol) in hexane while maintaining the temperature below −65° C. Upon completion of the addition the reaction mixture was maintained at −78° C. for an additional 45 minutes, after which time a solution of hexachloroethane (279 g, 1.18 mol) in tetrahydrofuran (120 mL) was added dropwise. The reaction mixture was maintained for an hour at −78° C., warmed to −20° C. and then quenched with water (1 L). The reaction mixture was extracted with methylene chloride (4×500 mL); the organic extracts were dried over magnesium sulfate and concentrated. The crude product was further purified by chromatography on silica gel using methylene chloride as eluent to afford the title product compound as a yellow oil (160 g).
후처리
- temperaturewhile maintaining the temperature below −65° C
- additionUpon completion of the addition the reaction mixture
- temperatureThe reaction mixture was maintained for an hour at −78° C.
- temperaturewarmed to −20° C.
- customquenched with water (1 L)
- extractionThe reaction mixture was extracted with methylene chloride (4×500 mL)
- dry with materialthe organic extracts were dried over magnesium sulfate
- concentrationconcentrated
- customThe crude product was further purified by chromatography on silica gel
출처 및 근거
- ORD 기록
- ord-9657c2a711e3481a9f253b225c851a9f
- 출처 데이터셋
- uspto-grants-2009_07
- 특허 번호
- US07560564B2
연결된 노트
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