HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 246643Erstellt: 25. Oktober 2026
Tributyltin Chloride → 6-chloro-3-(tributylstannyl)-1H-indazole
https://huagongshe.com/reaction/246643
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tributyltin Chloride | HCID 15096 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | HCID 178418918 | HCID 178418918 | — |
| Edukt | HCID 178477877 | HCID 178477877 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6-chloro-3-(tributylstannyl)-1H-indazole | HCID 178448229 | 77,3% |
Reaktionsschritte
To a solution of 6-chloro-3-iodo-1H-indazole (337 mg, 1.21 mmol) in dry tetrahydrofuran (20 mL) was added drop-wise isopropylmagnesium chloride (1.33 mL, 2M in THF, 2.66 mmol) at −16° C. under N2 atmosphere. After stirring for 20 minutes, tributylchlorostannane (472 mg, 1.45 mmol) was added drop-wise at −16° C., and then it was warmed to 20° C. for 2 h. Then NH4Cl solution (2 mL) was added and product extracted with dichloromethane (15 mL), organic phase was washed with water (2×20 mL) and brine (2×20 mL). The organic layer was dried over Na2SO4, filtered and concentrated to afford 6-chloro-3-(tributylstannyl)-1H-indazole (413 mg, crude) as yellow oil which was used to next step 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-7c2d1e5327cb4a3e848a01d9cf4525d5 |
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| Quellennotiz | uspto-grants-2014_02 |
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