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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216363Generated: October 25, 2026

Tributyltin Chloride → 1-Methyl-5-(tributylstannyl)-1H-pyrazole

https://huagongshe.com/reaction/216363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant1H-Pyrazole, 1-methyl-HCID 70255—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-5-(tributylstannyl)-1H-pyrazoleHCID 21867455—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Lithium diisopropylamide (1.5 M in cyclohexane) (9.7 mL, 14.6 mmol) was added to a −78° C. solution of 1-methylpyrazole (1 g, 12.2 mmol) in tetrahydrofuran (15 mL). After stirring at −78° C. for 15 min, chloro-tri-n-butylstannane (3.9 mL, 14.6 mmol) was added dropwise. The reaction mixture was allowed to warm to ambient temperature overnight. The reaction mixture was quenched with saturated aqueous ammonium chloride, diluted with water and extracted with ethyl acetate. The combined organic extracts were dried (magnesium sulfate), filtered and concentrated in vacuo. Chromatography over silica eluting with 0-100 ethyl acetate/hexane afforded 1-methyl-5-(tributylstannyl)-1H-pyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193228B2
Source datasetuspto-grants-2012_06
ORD IDord-8314bb2997214012b96ae829d21c7b06
Source noteuspto-grants-2012_06