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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441569Generated: November 1, 2026

Tributyltin Chloride → HCID 59164465, compound

https://huagongshe.com/reaction/1441569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantHCID 59164412HCID 59164412—
ReactantHCID 59164512HCID 59164512—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59164465HCID 5916446524%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution containing a 1:1 mixture of 3-methyl-1-(2-trimethylsilanylmethoxy-ethyl)-1H-pyrazole and 5-methyl-1-(2-trimethylsilanylmethoxy-ethyl)-1H-pyrazole (1.5 g, 7.06 mmol) in THF (20 mL) at −78° C. was added dropwise n-BuLi (1.6M in hexanes, 4.4 mL, 1 equiv) while keeping the temperature below −70° C. The mixture was then stirred 30 min at −78° C. prior to the addition of tributyltin chloride (1.9 mL, 1 equiv) (the temperature was maintained below −70° C.). The mixture was stirred at −78° C. for 30 min and for 2 h at r.t. Hexanes was added to the mixture and the insoluble material was removed by filtration. Concentration of the solution in vacuo gave a colorless syrup. The crude product was purified by flash chromatography (hexanes to EtOAc/hexanes (20/80)) to provide 3-methyl-5-tributylstannanyl-1-(2-trimethylsilanylmethoxy-ethyl)-1H-pyrazole (847 mg, 24%) as a colorless syrup. (TLC rf 0.33 in EtOAc/hexanes 5:95).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655666B2
Source datasetuspto-grants-2010_02
ORD IDord-4bf7291715a84093a838bbe90aaa9135
Source noteuspto-grants-2010_02