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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34470Erstellt: 24. Oktober 2026

Acetic Acid → Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoate

https://huagongshe.com/de/reaction/34470

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBromocresol GreenHCID 6451—
EduktSodium cyanoborohydrideHCID 5003444—
EduktEthyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoateHCID 54507081—
LösungsmittelEthanolHCID 702—
ProduktEthyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoateHCID 20129780—

Reaktionsschritte

A mixture of ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoate (19.8 g, 0.63 mole) in ethanol (500 mL) under nitrogen was treated with acetic acid (4 mL) and a trace of bromocresol green and heated to reflux. Heating was discontinued and sodium cyanoborohydride (4.4 g, 0.07 mole) in ethanol (100 mL) was co-added with additional acetic acid (11 mL). The mixture was stirred under nitrogen for 2 hr, acetic acid (10 mL) added and the ethanol removed under reduced pressure. The resultant yellow solid was taken up in ethyl acetate (250 mL) and successively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL), then dried over magnesium sulfate. The volatiles were removed under reduced pressure to leave an amber oil, 18.22 g (91.4%) which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04761475
Quelldatensatzuspto-grants-1988_08
ORD IDord-62b182c93158406b8248468834a06f6a
Quellennotizuspto-grants-1988_08