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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 622339Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/622339

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAndrosta-1,4-diene-3,17-dioneHCID 13472—
EduktN-bromobutanimideHCID 67184—
KatalysatorBenzoyl PeroxideHCID 7187—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt(8R,9S,10R,13S,14S)-6-bromo-10,13-dimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene-3,17-dioneHCID 2514113476,7%

Reaktionsschritte

A solution of 10 g of androsta-1,4-diene-3,17-dione in 95 ml of carbon tetrachloride is refluxed with 6.4 g of N-bromosuccinimide and 0.4 g of benzoyl peroxide for seventy five minutes. After filtration of succinimide, the filtrate was cooled in ice until crystallization is complete. The mixture is then filtered and dried so obtaining 9.8 g of crude 6-bromoandrosta-1,4-diene-3,17-dione satisfactory for the next step. The analytical sample is crystallized from diethyl ether/n-hexane, m.p. 188°-190° C., [α]D20° +116, U.V. (95% EtOH) λmax=250 nm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04771043
Quelldatensatzuspto-grants-1988_09
ORD IDord-153aaf94010a4abcb7b32c5ce37ac451
Quellennotizuspto-grants-1988_09