HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906573Generated: October 27, 2026
Tributyltin Chloride → 1-Isopropyl-5-tributylstannanyl-1H-pyrazole
https://huagongshe.com/reaction/906573
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-isopropyl-1H-pyrazole | HCID 13469816 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Isopropyl-5-tributylstannanyl-1H-pyrazole | HCID 59164521 | 82% |
Reaction Steps
To a cold (−78° C.) solution of LDA (prepared from n-BuLi (7.99 mL, 1.6 M, 1.1 eq) and diisopropylamine (1.82 mL, 1.1 eq)) in THF, a solution of 1-isopropyl-1H-pyrazole (1.28 g, 11.6 mmol) in THF was added dropwise while keeping the temperature below −70° C. At the end of the addition, the mixture was stirred at −78° C. for 30 min. Tributyltin chloride (3.44 mL, 1.1 eq) was then added dropwise while keeping the temperature below −70° C. At the end of the addition, the mixture was stirred for 1 h at −78° C. and for 2 h at r.t. The solvent was removed in vacuo and the crude oil was dissolved into AcOEt. The organic phase was washed with water and dried over Na2SO4. The solution was concentrated in vacuo to afford a yellow oil (3.82 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012988B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a0f223fed83c4e4db51374ca18926250 |
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| Source note | uspto-grants-2011_09 |
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