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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350713Generated: October 29, 2026

1-Methylimidazole → 1-Methyl-5-(tri-n-butylstannyl)imidazole

https://huagongshe.com/reaction/1350713

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantTributyltin ChlorideHCID 15096—
ReactantButyllithiumHCID 178418339—
Product1-Methyl-5-(tri-n-butylstannyl)imidazoleHCID 109156518.8%

Reaction Steps

Butyllithium (3.75 mL, 9.40 mmol) and TMEDA (2.24 mL, 14.85 mmol) were stirred at −20° C. in hexanes (7 mL) in an ethanol/dry ice/water bath for 30 minutes. 1-Methylimidazole (0.5 mL, 6.27 mmol) was added and the mixture stirred at room temperature for 1 h. After cooling to −20° C., Bu3SnCl (1.70 mL, 15.67 mmol) was added dropwise. The reaction stirred for 15 minutes at −20° C. then at room temperature overnight before being quenched with 1:1 EtOAc/water (20 mL). The layers were separated and the aqueous layer extracted with EtOAc (3×). The combined organics were washed with water, dried over Na2SO4, concentrated, and chromatographed (4:96 MeOH/EtOAc) to give 1-methyl-5-tributylstannanyl-1H-imidazole (0.486 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214802B2
Source datasetuspto-grants-2007_05
ORD IDord-bfb644dcc1d04a6aba5a85f2c3c45c81
Source noteuspto-grants-2007_05