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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343303Erstellt: 25. Oktober 2026

2-Formyl-17beta-estradiol → 3-Hydroxyestra-1,3,5(10)-trien-17-one-2-carboxaldehyde

https://huagongshe.com/reaction/343303

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Formyl-17beta-estradiolHCID 9994980—
EduktJones' reagentHCID 131709961—
LösungsmittelAcetoneHCID 180—
Produkt3-Hydroxyestra-1,3,5(10)-trien-17-one-2-carboxaldehydeHCID 1140378662%

Reaktionsschritte

To a solution of 3,17β-dihydroxyestra-1,3,5(10)-triene-2-carboxaldehyde (2a, 0.300 g, 1.0 mmol) in acetone (20 mL) was added Jones reagent (0.5 mL) at 0° C. The reaction mixture was stirred for 5 min, then quenched with 2-propanol, and extracted with EtOAc. The combined organic layers were washed with H2O, then with saturated aqueous NaCl, and dried (MgSO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was purified by column chromatography (silica gel) using n-hexane:THF (4:1→3:1, v/v) to approximately 0.185 g of 5 (62% yield), m.p. 154°-157° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05861388
Quelldatensatzuspto-grants-1999_01
ORD IDord-a8501990f77f478391e18e93927f23a9
Quellennotizuspto-grants-1999_01