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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779450Generated: November 2, 2026

3-Isopropoxy-4-(tri-n-butylstannyl)-3-cyclobutene-1,2-dione → HCID 86750789, compound

https://huagongshe.com/reaction/1779450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Isopropoxy-4-(tri-n-butylstannyl)-3-cyclobutene-1,2-dioneHCID 2736683—
ReactantHCID 67707702HCID 67707702—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 86750789HCID 8675078948.9%

Reaction Steps

A mixture of the product of Example 30 (c) (0.8 g), 3-isopropoxy-4-tributylstannylcyclobut-3-ene-1,2-dione (0.9 g), tetrakis(triphenylphosphine)palladium(0) (0.2 g), cuprous iodide (0.1 g) and dry dimethylformamide (5 ml) was stirred at ambient temperature under a nitrogen atmosphere for approximately 17 hours. The solvent was evaporated under reduced pressure and the resulting residue was dissolved in diethyl ether (150 ml). The solution obtained was washed with saturated aqueous ammonium chloride solution (50 ml), then with saturated aqueous potassium fluoride solution (2×50 ml) and then dried over magnesium sulphate. The solvent was evaporated and the residue obtained was purified by flash chromatography on silica gel (eluting with dichloromethane/methanol (50:1)) to give the intermediate compound (E)-methyl 2-benzyl-3-[2-butyl-4-chloro-1-[4-(2-isopropoxy-3,4-dioxocyclobut-1-en-1-yl)benzyl]-1H-imidazol-5-yl]propenoate as an oil (0.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627191
Source datasetuspto-grants-1997_05
ORD IDord-146bf441f1ed49b0b589a6c719bff2c2
Source noteuspto-grants-1997_05