Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1886089Erstellt: 25. Oktober 2026

MeOH tetrahydrofuran → 3-(3-Carbomethoxyphenyl)methyl-6-hydroxy-4-chromanone

https://huagongshe.com/reaction/1886089

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMeOH tetrahydrofuranHCID 21899815—
Edukt6-Benzyloxy-3-(3-carboxyphenylmethylene)-4-chromanoneHCID 54569724—
KatalysatorPalladiumHCID 23938—
Produkt3-(3-Carbomethoxyphenyl)methyl-6-hydroxy-4-chromanoneHCID 1909146463%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 6-benzyloxy-3-)3-carboxyphenylmethylene)-4-chromanone from Step 2 (1.54 g, 3.8 mmol) in 40 ml THF/MeOH (1:3) was added 150 mg of 10% Pd/C. The mixture was hydrogenated at 40 psi for 20 hr. The mixture was filtered through celite. The filtrate was evaporated to dryness and redissolved in THF. The THF solution was cooled to 0° C. and diazomethane was added until no acid remained. Then HOAc was added. The mixture was evaporated to give an oil which was chromatographed on silica gel and eluted with 40% EtOAc/hexane to give 750 mg (63%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05149703
Quelldatensatzuspto-grants-1992_09
ORD IDord-868f1ff3530a48ca81e46e55f6c0116d
Quellennotizuspto-grants-1992_09