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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017002Generated: October 26, 2026

Toluene → 3-(Furan-3-yl)benzaldehyde

https://huagongshe.com/reaction/1017002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromofuranHCID 89164—
Reactant3-Formylphenylboronic acidHCID 2734356—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(Furan-3-yl)benzaldehydeHCID 2350601010%

Reaction Steps

EX-601A) To a toluene (10 mL) solution of 3-bromofuran (0.54 mL, 6.0 mmol) was added 3-formylphenylboronic acid (1.00 g, 6.7 mmol) and DMF (4 mL). To the resulting solution was added K2CO3 (1.85 g, 13.4 mmol) and Pd(PPh3)4 (0.40 g, 0.35 mmol). The slurry was heated to reflux under argon for 2 h. The cooled mixture was poured into water and extracted with ethyl acetate. The organic layer was 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 0.10 g (10%) of the desired 3-(3-furanyl)benzaldehyde product as a yellow oil. MS: m/z=173.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476057B1
Source datasetuspto-grants-2002_11
ORD IDord-0e96dedeb2db434abd0ebaa704af1346
Source noteuspto-grants-2002_11