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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 597440Erstellt: 24. Oktober 2026

Dehydroepiandrosterone → 11beta-Hydroxyestradiol

https://huagongshe.com/de/reaction/597440

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDehydroepiandrosteroneHCID 5881—
EduktProgesteroneHCID 5994—
EduktPregnenoloneHCID 8955—
EduktAndrostenediolHCID 10634—
EduktDihydroandrostenedioneHCID 222865—
Edukt5alpha-Androstane-3beta,17beta-diolHCID 242332—
Edukt19-Nor-5-androstenediolHCID 9900246—
Edukt19-NordehydroepiandrosteroneHCID 53990402—
Produkt11beta-HydroxyestradiolHCID 227673—

Reaktionsschritte

This reduction procedure is useful for the preparation of the 11α-acid succinates of 11α-hydroxy analogs of dehydroepiandrosterone, pregnenolone, progesterone, 3β-hydroxy-estr-5-en-17-one, and 5α-androstane-3,17-dione to 11α-hydroxy succinate derivatives of androst-5-ene-3β,17β-diol, pregn-5-ene-3β,20α and 20β diols, pregn-4-ene-3,20α and 20β diols, estr-5-en-3β,17β-diol and 5α-androstane-3β,17β-diol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04013688
Quelldatensatzuspto-grants-1977_03
ORD IDord-ce7257e7003f4e99b1e7535e164b02fd
Quellennotizuspto-grants-1977_03