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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898642Generated: October 30, 2026

Tributyltin Chloride → 4-tributylstannanyl-1-(2,3,5-trifluoro-phenyl)-1H-imidazole

https://huagongshe.com/reaction/1898642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-iodo-1-(2,3,5-trifluorophenyl)-1H-imidazoleHCID 57516655—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product4-tributylstannanyl-1-(2,3,5-trifluoro-phenyl)-1H-imidazoleHCID 57516656—

Reaction Steps

A solution of 4-iodo-1-(2,3,5-trifluorophenyl)-1H-imidazole (0.140 g, 0.43 mmol) in 2 mL of THF under Ar was chilled in an ice/water bath 5 min. Isopropylmagnesium chloride (2.0 M in tetrahydrofuran, 0.225 mL, 0.45 mmol) was added, the bath was removed, and the pale yellow solution was stirred for 1.5 h. Tributyltin chloride (0.055 mL, 0.20 mmol) was added all at once, and the pale yellow solution was stirred 1 h. A sat. aq. NH4Cl solution (10 mL) was added, and the mixture was extracted with two 10 mL portions of EtOAc. The combined organic layers were washed with 10 mL of a sat. aq. NaCl solution, dried over Na2SO4, filtered and concentrated to give 4-tributylstannanyl-1-(2,3,5-trifluoro-phenyl)-1H-imidazole as a yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518945B2
Source datasetuspto-grants-2013_08
ORD IDord-4d86e693c3334ad7bcc2806afed3319a
Source noteuspto-grants-2013_08