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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130905Erstellt: 25. Oktober 2026

Hydrogen Peroxide → Ammonium Bicarbonate

https://huagongshe.com/reaction/130905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktIsoamylamineHCID 7894—
EduktEthylvanillinHCID 8467—
EduktPotassium CarbonateHCID 11430—
Edukt4-FluorobenzonitrileHCID 14517—
LösungsmittelDimethylformamideHCID 6228—
ProduktAmmonium BicarbonateHCID 14013—
ProduktHCID 59729983HCID 59729983—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

Dissolve 3-ethoxy-4-hydroxy-benzaldehyde (2.57 g, 15.45 mmol) in DMF (20 mL), add K2CO3 (2.33 g, 16.86 mmol) and 4-fluorobenzonitrile (1.70 g, 14.05 mmol), heat the mixture at 130° C. overnight. Add water and extract the aqueous layer with EtOAc. Combine organic layers and dry over Na2SO4. Eliminate the solvent and purify by flash chromatography on silica gel (eluent: EtOAc/hexane 15/85) to get a mixture of two compounds (1.45 g). This mixture (240 mg) is submitted to the reductive amination conditions described for compound 1 (step 3) using 3-methyl-butylamine to obtain a mixture of two compounds which is subject to hydrolysis using hydrogen peroxide and potassium carbonate in the conditions described elsewhere in this document. This mixture is purified by flash chromatography (EtOAc and CH2Cl2/MeOH 10%) and then the title compound is isolated after HPLC (Column: XTerraMSC18 (5 um, 19×100 mm). Isocratic mode: 55/45 Ammonium bicarbonate-pH 9-/Acetonitrile. Flow: 10 mL/min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381719B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-cc0e8454054e4ccdb4c60b683943b774
Quellennotizuspto-grants-2008_06