HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 246296Erstellt: 23. Oktober 2026
Tributyltin Chloride → 5-(difluoromethoxy)-3-(tributylstannyl)-1H-indazole
https://huagongshe.com/de/reaction/246296
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tributyltin Chloride | HCID 15096 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | HCID 178418918 | HCID 178418918 | — |
| Edukt | HCID 178506407 | HCID 178506407 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-(difluoromethoxy)-3-(tributylstannyl)-1H-indazole | HCID 178448231 | — |
Reaktionsschritte
In a round-bottomed flask, 5-difluoromethoxy-3-iodo-1H-indazole (200 mg, 0.6 mmol) was dissolved in THF (3.6 ml) and sodium hydride (60% in mineral oil, 64 mg, 1.6 mmol) was added. The reaction mixture was stirred at room temperature for 10 min then cooled to −16° C. (NaCl/ice bath) and isopropylmagnesium chloride (2.0 M in THF, 0.46 ml, 0.920 mmol) was added dropwise. The reaction mixture was stirred at −16° C. for 30 min then tributylchlorostannane (0.22 ml, 0.81 mmol) was slowly added. The reaction mixture was allowed to warm to room temperature and stirred for 1 h then quenched with saturated NH4Cl— solution and extracted with EtOAc (2×). The combined organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated to give 5-difluoromethoxy-3-tributylstannanyl-1H-indazole as a yellow oil which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08658646B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-3231c251bbf74a25b3612b670df47680 |
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| Quellennotiz | uspto-grants-2014_02 |
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