HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216363Erstellt: 25. Oktober 2026
Tributyltin Chloride → 1-Methyl-5-(tributylstannyl)-1H-pyrazole
https://huagongshe.com/reaction/216363
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Tributyltin Chloride | HCID 15096 | — |
| Edukt | 1H-Pyrazole, 1-methyl- | HCID 70255 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Methyl-5-(tributylstannyl)-1H-pyrazole | HCID 21867455 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08193228B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-8314bb2997214012b96ae829d21c7b06 |
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| Quellennotiz | uspto-grants-2012_06 |
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