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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012525Generated: October 30, 2026

2-(Tri-n-butylstannyl)thiophene → HCID 66974643, compound

https://huagongshe.com/reaction/1012525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
Reactanttert-Butyl {[5-bromo-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 57522258—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 66974643HCID 6697464373%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of crude tributyl(2-thienyl)stannane (1.1 g) and tert-butyl{[5-bromo-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamate (430 mg) in toluene was added tetrakis(triphenylphosphine)palladium (116 mg), and the mixture was stirred under a nitrogen atmosphere at 120° C. for 1 hr. The reaction mixture was allowed to cool to room temperature and the solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent:hexane-ethyl acetate=4:1) to give the title compound as a pale-yellow oil (yield 315 mg, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977488B2
Source datasetuspto-grants-2011_07
ORD IDord-9ce62c82f0cc45c6a3ec496493593ff7
Source noteuspto-grants-2011_07