Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602305Generated: October 31, 2026

2-(Tributylstannyl)furan → HCID 9881902, compound

https://huagongshe.com/reaction/1602305

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
Reactant5-Bromo-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furanHCID 10779312—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 9881902HCID 988190243.5%

Reaction Steps

A mixture of 5-bromo-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furan (1.13 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 of 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 0.47 g (43%) of the title compound as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981547
Source datasetuspto-grants-1999_11
ORD IDord-3e57afd5e96e4d54850fda2219a595d3
Source noteuspto-grants-1999_11