참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tributyltin Chloride | HCID 15096 | — |
| 반응물 | 1H-Pyrazole, 1-methyl- | HCID 70255 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Methyl-5-(tributylstannyl)-1H-pyrazole | HCID 21867455 | — |
반응 단계
Lithium diisopropylamide (1.5 M in cyclohexane) (9.7 mL, 14.6 mmol) was added to a −78° C. solution of 1-methylpyrazole (1 g, 12.2 mmol) in tetrahydrofuran (15 mL). After stirring at −78° C. for 15 min, chloro-tri-n-butylstannane (3.9 mL, 14.6 mmol) was added dropwise. The reaction mixture was allowed to warm to ambient temperature overnight. The reaction mixture was quenched with saturated aqueous ammonium chloride, diluted with water and extracted with ethyl acetate. The combined organic extracts were dried (magnesium sulfate), filtered and concentrated in vacuo. Chromatography over silica eluting with 0-100 ethyl acetate/hexane afforded 1-methyl-5-(tributylstannyl)-1H-pyrazole.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08193228B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-8314bb2997214012b96ae829d21c7b06 |
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| 출처 메모 | uspto-grants-2012_06 |
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