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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1047993Erstellt: 24. Oktober 2026

Ethyl Acetate → HCID 67080394, Verbindung

https://huagongshe.com/de/reaction/1047993

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktTrimethylsilyl cyanideHCID 82115—
Edukt7-fluoro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-oneHCID 15205373—
Katalysatorzinc(II)iodideHCID 9883512—
LösungsmittelHydrochloric AcidHCID 313—
ProduktHCID 67080394HCID 6708039424,25%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To 7-fluoro-2,2-dimethyl-2,3-dihydrochromen-4-one (1.000 g, 5.149 mmol) was added trimethylsilyl cyanide (3.215 mL, 25.75 mmol) followed by a spatula tip of zinc iodide. The reaction was heated at 50° C. for 1 hour. The reaction was cooled, diluted with ethyl acetate (40 mL) and washed with saturated sodium bicarbonate (2×25 mL), brine (25 mL), dried over magnesium sulfate and concentrated. The product was dissolved in 5 mL of acetic acid and 5 mL of HCl, and SnCl2 dihydrate (4.648 g, 20.60 mmol) was added. The reaction heated at reflux (130° C. oil bath temperature) overnight. The reaction was cooled, diluted with ethyl acetate (50 mL), washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate and concentrated. The residue was purified by silica gel chromatography over silica gel eluting with a gradient of 0.5% MeOH/CH2Cl2 containing 0.5% acetic acid to 10% MeOH/CH2Cl2 containing 0.5% acetic acid to provide the title compound (0.280 g, 24.25% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08569522B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-f2a1ae2eb6044a61916da20f9cb8f8f6
Quellennotizuspto-grants-2013_10