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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50486Generated: October 27, 2026

1,4-Dioxane → 3-(2-Furanyl)4-(4-morpholinyl)benzaldehyde

https://huagongshe.com/reaction/50486

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium FluorideHCID 522689—
Reactant2-(Tributylstannyl)furanHCID 4393688—
Reactant3-Bromo-4-morpholinobenzaldehydeHCID 23506020—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
Product3-(2-Furanyl)4-(4-morpholinyl)benzaldehydeHCID 2350603684%

Reaction Steps

EX-604B) To a dioxane (8 mL) solution of the aldehyde from EX-604A (0.77 g, 2.8 mmol) was added 2-(tributylstannyl)furan (1.07 mL, 3.42 mmol) and Pd(PPh3)2Cl2 (0.12 g, 0.17 mmol). The mixture was heated to reflux under argon for 18 h. The cooled mixture was poured into a mixture of saturated aq. KF and ethyl acetate and stirred 3 h. The slurry was filtered through celite. The organic layer was separated, washed with brine, dried (MgSO4) and evaporated to a yellow oil. Purification by silica gel flash chromatography eluting with 20% ethyl acetate in hexane gave 0.61 g (84%) of the desired 3-(2-furanyl)4-(4-morpholinyl)benzaldehyde product as a yellow oil. MS: m/z=258.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710089B2
Source datasetuspto-grants-2004_03
ORD IDord-00daf0f797e04c8594831611bfd26551
Source noteuspto-grants-2004_03