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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1357475Erstellt: 26. Oktober 2026

Isopropenyl acetate → 2-Methoxy-3,17-diacetoxyestra-1,3,5(10),14,16-pentaene

https://huagongshe.com/reaction/1357475

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropenyl acetateHCID 7916—
EduktAcetic AnhydrideHCID 7918—
Edukt2-Methylbenzenesulfonic acid hydrateHCID 12496995—
Edukt2-Methoxyestra-1,3,5(10),15-tetraen-3-ol-17-oneHCID 21135701—
LösungsmittelAcetoneHCID 180—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Methoxy-3,17-diacetoxyestra-1,3,5(10),14,16-pentaeneHCID 1132653180,8%

Reaktionsschritte

Under nitrogen, toluenesulfonic acid monohydrate (0.1 g, 0.53 mmol) was added to a solution of 2-Methoxyestra-1,3,5(10),15-tetraen-3-ol-17-one prepared in Example 3 (0.25 g, 0.84 mmol), isopropenyl acetate (5 mL, 45.15 mmol) and acetic anhydride (5 mL, 53 mmol) and the mixture was heated to reflux for 6 h. At the end of that time, analysis by tlc (2% acetone in CH2Cl2) indicated a complete reaction. The reaction was cooled to room temperature, poured into ice water (˜100 mL) and stirred for 1 h. The mixture was extracted with methylene chloride (3x). The organic fractions were washed with water (1x), saturated sodium bicarbonate solution (1x) and water (1x), filtered through anhydrous sodium sulfate, combined and concentrated in vacuo. The residue was crystallized from methanol to give the pure diacetate (17) (0.259 g, 80.8%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06593321B2
Quelldatensatzuspto-grants-2003_07
ORD IDord-b12bbfe5a68b46f382406ef47271b6fb
Quellennotizuspto-grants-2003_07