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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50478Generated: October 25, 2026

1,4-Dioxane → Ketone, 3-furyl phenyl

https://huagongshe.com/reaction/50478

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 numberUS06710089B2
Source datasetuspto-grants-2004_03
ORD IDord-c7218a36617a4189acd66a0662a36453
Source noteuspto-grants-2004_03