HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246395Generated: October 25, 2026
Tributyltin Chloride → 5-(difluoromethoxy)-3-(tributylstannyl)-1H-indazole
https://huagongshe.com/reaction/246395
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Reactant | HCID 178506407 | HCID 178506407 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(difluoromethoxy)-3-(tributylstannyl)-1H-indazole | HCID 178448231 | — |
Reaction Steps
5-(Difluoromethoxy)-3-iodo-1H-indazole (0.175 g, 564 μmol) was dissolved in THF (3 mL). The colorless solution was cooled to −16° C. (NaCl/ice bath), isopropylmagnesium chloride 2M in THF (621 μL, 1.24 mmol.2) was added dropwise at −16° C. The reaction mixture was stirred at −16° C. for 20 min. Then, tributylchlorostannane (220 mg, 184 μL, 677 μmol.2) was added slowly. The reaction mixture was warmed to 25° C. and stirred for 1.5 h. The reaction mixture was quenched with saturated ammonium chloride solution, extracted with dichloromethane (3×30 mL), organics dried over MgSO4 and concentrated to a yellow oil. The residue was dried under high vacuum and taken into next step without further purification yielding 5-(difluoromethoxy)-3-(tributylstannyl)-1H-indazole, crude mass exceeded yield, assumed quantitative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658646B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-66df65a524724eaa81d34867f07331db |
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| Source note | uspto-grants-2014_02 |
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