HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635886Generated: November 2, 2026
Tributyltin Chloride → 1-Methyl-4-(tributylstannyl)-1H-pyrazole
https://huagongshe.com/reaction/1635886
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 1H-Pyrazole, 4-bromo-1-methyl- | HCID 167433 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Methyl-4-(tributylstannyl)-1H-pyrazole | HCID 10571238 | — |
Reaction Steps
To a precooled (<−10° C. internal temperature) solution of 1.6M n-butyl lithium in hexanes (100 ml) in anhydrous diethyl ether (100 ml) under argon was added a solution of 4-bromo-1-methyl-1H-pyrazole (23.42 g) from Example 111 in diethyl ether (50 ml) at a rate to maintain the temperature. The reaction was allowed to stir for a further 20 minutes before tributyltin chloride (43.4 ml) was added in diethyl ether (50 ml). The reaction temperature was allowed to rise to 20° C. The reaction was diluted with diethyl ether and the insoluble material removed by suction filtration. Evaporation of the solvent in vacuo afforded 56 g of the title compound as an oil. MS, m/z: 373 [M+H]+. Residual amounts of tin residues were removed from the oil by distillation using a kugelrohr apparatus under high vacuum at 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06511974B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-2b490def57ba4c23ba3ed975d521c983 |
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| Source note | uspto-grants-2003_01 |
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