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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 637618Erstellt: 25. Oktober 2026

Acetic Acid → 7alpha-Methylestr-4-ene-3,11,17-trione

https://huagongshe.com/reaction/637618

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktMethaneHCID 297—
EduktSulfuric AcidHCID 1118—
Edukt11alpha-Hydroxy-7alpha-methylestr-4-ene-3,17-dioneHCID 12020273—
KatalysatorWaterHCID 962—
KatalysatorManganese sulfate monohydrateHCID 177577—
Katalysatorchromium (VI) trioxideHCID 10219390—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethane ethylacetateHCID 21226138—
Produkt7alpha-Methylestr-4-ene-3,11,17-trioneHCID 57277685—

Reaktionsschritte

A mixture of 11α-hydroxy-7α-methylestr-4-ene-3,17-dione (A, obtained from Fermentation) and acetic acid (7.5 ml) is stirred and cooled to about 10° in a cold water bath. The following reagents are added: water (6 drops), manganese sulfate monohydrate (0.1 g) in water (1 ml), chromium trioxide (0.66 g) in water (2 ml), and concentrated sulfuric acid (0.6 ml). The chromium trioxide solution is added over a 15 minute period. After 1/2 hour water (10 ml) is added and the crystals of the product are collected, washed with water and dried to give a solid. The solid is dissolved in hot ethyl acetate/methylene chloride (1/1) and decolorized with a little charcoal and silica gel and then filtered through celite. The appropriate fractions are pooled and concentrated to give crystals, UV (ethyl alcohol) λmax =239 nm (ε=16250); IR (mull) 1740, 1707, 1672 and 1616; MS (m/e)=300, 282, 272, and 258.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04557867
Quelldatensatzuspto-grants-1985_12
ORD IDord-ef76c2cfb25c45848d5eb8ad055c7b8e
Quellennotizuspto-grants-1985_12