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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 554203Erstellt: 23. Oktober 2026

Methanol → HCID 57522146, Verbindung

https://huagongshe.com/de/reaction/554203

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktWaterHCID 962—
EduktMethylamineHCID 6329—
EduktSodium borohydrideHCID 4311764—
Edukt5-Phenyl-1H-pyrrole-3-carboxaldehydeHCID 11052090—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktHCID 57522146HCID 5752214664%

Reaktionsschritte

To a solution (92 mL) of 5-phenyl-1H-pyrrole-3-carbaldehyde (0.92 g) in methanol was added 40% methylamine solution (1.26 g) at room temperature and the mixture was stirred for 30 min. To the reaction mixture was added sodium borohydride (305 mg) at room temperature and the mixture was stirred for 10 min. Water (200 mL) was added and the mixture was further stirred for 1 hr. Saturated brine (50 mL) was added and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was dissolved in acetonitrile (48 mL), and di-tert-butyl bicarbonate (1.41 g) was added dropwise at room temperature. The mixture was stirred for 1.5 hr and partitioned with water and ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→4:1) to give the title compound as colorless crystals (yield 0.99 g, 64%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08048909B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-ac3ca403bcfe44e396a957ac40052656
Quellennotizuspto-grants-2011_11