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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174238Generated: November 1, 2026

Tributyltin Chloride → 5-Methyl-2-(tri-n-butylstannyl)pyridine

https://huagongshe.com/reaction/1174238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant2-Bromo-5-methylpyridineHCID 564216—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product5-Methyl-2-(tri-n-butylstannyl)pyridineHCID 11132711—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution containing 2-bromo-5-methylpyridine (1.42 g, 8.23 mmol) in ether (15 mL) at −78° C. was treated with n-butyllithium (5.14 mL, 1.6 M in hexanes) dropwise, stirred at −78° C. for 1 hour, treated with tributyltin chloride (3.35 mL, 12.35 mmol), stirred at 0° C. for 4 hours, quenched with saturated ammonium chloride solution and partitioned between ether and water. The organic phase was washed with brine and dried over MgSO4, filtered and concentrated. The residue was purified by chromatography on neutral alumina eluting with 10% ethyl acetate in dichloromethane to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834043B2
Source datasetuspto-grants-2010_11
ORD IDord-881f86760d1e4af1ad3ce9f0d54ea58d
Source noteuspto-grants-2010_11