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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086479Generated: October 31, 2026

Toluene → 3-(Furan-3-yl)benzaldehyde

https://huagongshe.com/reaction/2086479

Reaction equation

Participants

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

Reaction Steps

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 K2C03 (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 numberUS06723753B2
Source datasetuspto-grants-2004_04
ORD IDord-e17455a79f7f42fa89fd801ba7dd7a6b
Source noteuspto-grants-2004_04