Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478810Generated: October 31, 2026

Allyltributylstannane → HCID 118513273, compound

https://huagongshe.com/reaction/1478810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyltributylstannaneHCID 90628—
ReactantPotassium FluorideHCID 522689—
Reactant2-Bromo-4-(trifluoromethoxy)anilineHCID 688296—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 118513273HCID 118513273—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-bromo-4-(trifluoromethoxy)aniline (75 g, 293 mmol) in DMF (1000 ml) was added Pd(PPh3)4 (13.5 g, 11.7 mmol) and allyltributyltin (116 g, 351 mmol) and the reaction mixture was stirred at 80° C. for 16 h. The mixture was cooled to room temperature and saturated aqueous KF solution was added. The mixture was diluted with ethyl acetate (1500 mL) and washed with 1:1 H2O: saturated aqueous NaCl solution (2×750 mL) and saturated aqueous KF (1×). The aqueous layers were combined and extracted with ethyl acetate (250 mL). The organic extracts were combined, dried over MgSO4, filtered and concentrated under reduced pressure to give the crude product, which was absorbed onto silica and purified by chromatography eluting with 1% ethyl acetate in petroleum ether to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403833B2
Source datasetuspto-grants-2016_08
ORD IDord-f425d8fc753946928caa289c6725d5a9
Source noteuspto-grants-2016_08