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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355371Generated: October 25, 2026

Tributyltin Chloride → 1-methyl-5-(tributylstannyl)-1H-1,2,3-triazole

https://huagongshe.com/reaction/355371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant1-Methyl-1H-1,2,3-triazoleHCID 140119—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product1-methyl-5-(tributylstannyl)-1H-1,2,3-triazoleHCID 2260982665.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1-methyl-1H-[1,2,3]triazole (350 mg) in dry tetrahydrofuran (5.0 ml) was added dropwise under nitrogen to a stirred, cooled (-78° C.) solution of n-butyl lithium (2.81 ml of 1.6M solution in hexanes) in dry tetrahydrofuran (10 ml). After 1 hour tributylchlorostannane (1.46 g) was added. The reaction was maintained at -78° C. for 30 min. and then allowed to warm to room temperature over 2 hours. The reaction mixture was diluted with brine (10 ml) and extracted into ethyl acetate (50 ml). The organic layer was separated, washed with brine (50 ml), dried over MgSO4, filtered and the solvent removed under reduced pressure. The residue was purified by flash column chromatography (20% ethyl acetate/n-hexane), to give 1-methyl-5-tributylstannanyl-1H-[1,2,3]triazole as a yellow oil (1.03 g). 1H NMR (360 MHz,CDCl3) δ 0.87 (9H, m), 1.15 (6H, m), 1.28 (6H, m), 1.36 (6H, m), 4.02 (3H, s), 7.60 (1H, s); MS m/z CI+ 372 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05830892
Source datasetuspto-grants-1998_11
ORD IDord-f9792f51fe524687b2d64ce493244239
Source noteuspto-grants-1998_11