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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216363Erstellt: 25. Oktober 2026

Tributyltin Chloride → 1-Methyl-5-(tributylstannyl)-1H-pyrazole

https://huagongshe.com/reaction/216363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributyltin ChlorideHCID 15096—
Edukt1H-Pyrazole, 1-methyl-HCID 70255—
EduktLithium diisopropylamideHCID 2724682—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Methyl-5-(tributylstannyl)-1H-pyrazoleHCID 21867455—

Reaktionsbedingungen

Temperatur-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193228B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-8314bb2997214012b96ae829d21c7b06
Quellennotizuspto-grants-2012_06