Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990467Generated: October 25, 2026

1,4-Dioxane → Ketone, 3-furyl phenyl

https://huagongshe.com/reaction/990467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantPotassium FluorideHCID 522689—
Reactant2-(Tributylstannyl)furanHCID 4393688—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
ProductKetone, 3-furyl phenylHCID 20164086%

Reaction Steps

EX-592A) To a dioxane (20 mL) solution of 3-bromobenzaldehyde (0.63 mL, 5.4 mmol) was added 2-(tributylstannyl)furan (1.89 mL, 6.00 mL) and Pd(PPh3)2Cl2 (0.21 g, 0.30 mmol). The mixture was heated to reflux under argon for 1.5 h. The cooled mixture was poured into a mixture of saturated KF and ethyl acetate and stirred 18 h. The slurry was filtered through celite. The organic layer was separated, washed with brine, dried (MgSO4) and evaporated to an oil. Purification by flash chromatography on silica gel eluting with 5% ethyl acetate in hexane gave 0.80 g (86%) of the desired 3-(2-furanyl)benzaldehyde product as an yellow oil which solidified upon standing. MS: m/z=173.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458849B1
Source datasetuspto-grants-2002_10
ORD IDord-e42df30744184910b4853ad088e78768
Source noteuspto-grants-2002_10