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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602310Generated: November 2, 2026

2-(Tributylstannyl)furan → HCID 19610968, compound

https://huagongshe.com/reaction/1602310

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
ReactantHCID 18689985HCID 18689985—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 19610968HCID 1961096840.1%

Reaction Steps

A mixture of 5-bromo-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]thiophene (1.20 g, 4.0 mmol), 2-(tributylstannyl)furan (1.71 g, 4.8 mmol), tetrakis(triphenylphosphine)palladium (0.46 g, 0.4 mmol), and 20 mL of toluene is heated under argon at reflux for 30 min. The reaction mixture is cooled to room temperature, concentrated in vacuo, diluted with ether, washed with 10% aqueous ammonium hydroxide solution and with brine, dried over anhydrous magnesium sulfate, and concentrated to give a dark oil. Purification by flash column chromatography on silica gel (1% ethyl acetate-hexane) yields about 0.46 g (40%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981547
Source datasetuspto-grants-1999_11
ORD IDord-55b60923b4ff4da6b82e28b069099621
Source noteuspto-grants-1999_11