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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2393209Erstellt: 25. Oktober 2026

3beta-Benzyloxy-5-androsten-17-one → 3beta-Methyl-5alpha-androstan-17-one

https://huagongshe.com/reaction/2393209

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3beta-Benzyloxy-5-androsten-17-oneHCID 53764908—
Edukt5alpha-Hydroperoxy-3beta-hydroxyandrost-6-en-17oneHCID 56628389—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelAcetic AcidHCID 176—
Produkt3beta-Methyl-5alpha-androstan-17-oneHCID 1863762780%

Reaktionsschritte

Firstly an example of catalytic hydrogenation for the synthesis of 5α-androstanes from androst-5-enes is the synthesis of 3β-methyl-5α-androstan-17-one 2 from 3β-methylandrost-5-en-17-one 1. 3β-Methylandrost-5-en-17-one 1 (400 mg), prepared as described previously was dissolved in glacial acetic acid (80 ml). Palladium on carbon (10%, 100 mg) was added and the solution maintained under an atmosphere of hydrogen. When hydrogen uptake ceased, the solution was filtered through celite and evaporated to give solid which was recrystallized from methanol to yield 3β-methyl-5α-androstan-17-one, 2, (320 mg, 80% yield). MP 107°-108° C., 1H NMR (CDCl3) δ0.86 (d, 3H, J-5Hz, methyl at C-3), 0.85 (s, 3H, C-19 Me), 0.79 (s, 3H, C-18 Me).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05804576
Quelldatensatzuspto-grants-1998_09
ORD IDord-9e37747326c444798f22a97ae83dcb7e
Quellennotizuspto-grants-1998_09