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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 915688Erstellt: 26. Oktober 2026

Potassium Carbonate → 3-Phenylfuran-2-carbaldehyde

https://huagongshe.com/reaction/915688

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktTriphenylphosphineHCID 11776—
EduktPhenylboronic AcidHCID 66827—
Edukt3-Bromo-2-furaldehydeHCID 3367271—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt3-Phenylfuran-2-carbaldehydeHCID 13465704107,4%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Prepare a mixture of 3-bromofuran-2-carbaldehyde (381 mg, 2.19 mmol), phenylboronic acid (534 mg, 4.38 mmol), and 2M potassium carbonate (3.28 mL, 6.57 mmol) in 1,2-dimethoxyethane (20 mL). Bubble nitrogen into this mixture for 20 minutes. Add Pd2(dba)3 (68 mg, 0.06 mmol) and PPh3 (68 mg, 0.26 mmol) and purge the mixture with nitrogen for an additional 10 minutes. Then heat the mixture to 80° C. After 24 hours, evaporate the solvent and redissolve the residue in ethyl acetate. Extract the aqueous phase with ethyl acetate (2×10 mL), wash the combined organic phases with brine (40 mL), dry (magnesium sulfate), filter and concentrate. Perform flash chromatography on silica gel eluting with 5:1 hex/ethyl acetate to afford 405 mg of the title compound as a white solid. MS: m/e=173 [MH+]

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07265246B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-da8fbbdf7e3c4730990c848a5e04d2f8
Quellennotizuspto-grants-2007_09