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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47239Erstellt: 23. Oktober 2026

Formaldehyde → HCID 68837732, Verbindung

https://huagongshe.com/de/reaction/47239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
Edukt3-MethoxypropylamineHCID 1672—
Edukt(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
ProduktHCID 68837732HCID 688377321%

Reaktionsschritte

A mixture of Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one (120.0 mg, 0.571 mmol), paraformaldehyde (17.1 mg, 0.571 mmol), and 3-methoxypropylamine (58.2 μL, 0.571 mmol) in 4.0 mL EtOH was heated at reflux for 6.5 h. The reaction mixture was cooled to room temperature and let stand for 22 h. The reaction mixture was filtered and the filter cake rinsed with 30% ethyl acetate in hexane. The filtrate was concentrated in vacuo and 4 ML of EtOH added. The reaction was refluxed an additional 19.5 h. The reaction mixture was cooled to room temperature and partitioned between 30 mL dilute HCl and 20 mL Ethyl acetate. The organic layer was removed and the aqueous layer washed with 15 mL ethyl acetate. The aqueous layer was made basic to pH 8 with saturated NaHCO3 and extracted with ethyl acetate. The ethyl acetate layer was washed with H2O, brine and dried over anhydrous Na2SO4. The ethyl acetate layer was filtered and then concentrated. The solid obtained (42.5 mg) was dissolved in CHCl3 and purified by chromatography (silica gel, 1:1/hexane:acetone) to give the title compound (1.5 mg, 1%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699863B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-2582b8a8a0d6406f90a949840fafd6f9
Quellennotizuspto-grants-2004_03