참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexachloroethane | HCID 6214 | — |
| 반응물 | N,N-dimethyl-1H-pyrazole-1-sulfonamide | HCID 10954038 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 3-Chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide | HCID 21113388 | — |
반응 단계
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-butyllithium (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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09445593B1 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-8f699849a5c84fca8d42d8812131cebc |
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| 출처 메모 | uspto-grants-2016_09 |
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