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HRID 1175662Erstellt: 27. Oktober 2026

Androsta-1,4-diene-3,17-dione → (8'R,9'S,10'R,13'S,14'S)-10',13'-dimethylspiro[1,3-dioxolane-2,17'-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene]-3'-one

https://huagongshe.com/reaction/1175662

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAndrosta-1,4-diene-3,17-dioneHCID 13472—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelEthylene GlycolHCID 174—
LösungsmittelBenzeneHCID 241—
Produkt(8'R,9'S,10'R,13'S,14'S)-10',13'-dimethylspiro[1,3-dioxolane-2,17'-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene]-3'-oneHCID 706103995%

Reaktionsschritte

To a solution of androsta-1,4-dien-3,17-dione (1, 10.0 g) in benzene (600 ml) and ethylene glycol (90 ml) was added toluene-p-sulfonic acid monohydrate (0.3 g), and the solution was refluxed for 8-10 hours with a Dean-Stark apparatus for collecting water. The reaction mixture was cooled to room temperature, diluted with ethyl acetate and washed thoroughly with water, dilute sodium bicarbonate solution, water and finally with brine. The organic phase was dried over anhydrous magnesium sulfate, filtered and the organic solvent removed by rotary evaporator. The resultant solid was crystallized from methanol to give 17,17-ethylenedioxyandrosta-1,4-dien-3-one (2) as a white crystalline solid in 95% yield (11.0 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07842680B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-7a8f0d035dc74027bce9ed0cff7c06b3
Quellennotizuspto-grants-2010_11