Acetic Anhydride → Nandrolone acetate

HRID 233467

Reaktionsgleichung

Reaktionsgleichung von HRID 233467
[CH3:1][C@@:2]12[C@@H:10]([OH:11])[CH2:9][CH2:8][C@H:7]1[C@@H:6]1[CH2:12][CH2:13][C:14]3[C@@H:20]([C@H:5]1[CH2:4][CH2:3]2)[CH2:19][CH2:18][C:16](=[O:17])[CH:15]=3.[C:21](OC(=O)C)(=[O:23])[CH3:22]>N1C=CC=CC=1.C(Cl)(=O)C>[CH3:22][C:21]([O:11][C@@H:10]1[C@@:2]2([CH3:1])[CH2:3][CH2:4][C@@H:5]3[C@@H:20]4[C:14](=[CH:15][C:16]([CH2:18][CH2:19]4)=[O:17])[CH2:13][CH2:12][C@H:6]3[C@@H:7]2[CH2:8][CH2:9]1)=[O:23]

Komponenten

5

Edukt 2

HCID 7918Acetic AnhydrideHCID 9904Nandrolone

Produkt 1

HCID 102122Nandrolone acetate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1049PyridineLösungsmittelHCID 6367Acetyl chlorideLösungsmittel

Versuchsvorschrift

In an apparatus supplied with a drierite drying tube, a solution of 19-nor-testosterone (6) (100 g; 0.365 mole) in acetic anhydride (200 ml), pyridine (32 ml) and acetylchloride (320 ml) was heated at reflux under magnetic stirring, for 3 h and then concentrated to dryness under vacuum. The dry residue was triturated in absolute ethanol, filtered and washed with little portions of absolute ethanol. After drying, 19-nortestosterone acetate 3-enolacetate was obtained as a white powder (121.4 g, yield 93%) mp. 176°-177° C. The structure was confirmed by spectroscopic means.

Aufarbeitung

  1. customIn an apparatus supplied with a drierite drying tube
  2. temperatureat reflux under magnetic stirring, for 3 h
  3. concentrationconcentrated to dryness under vacuum
  4. customThe dry residue was triturated in absolute ethanol
  5. filtrationfiltered
  6. washwashed with little portions of absolute ethanol
  7. customAfter drying

Quellen und Nachweise

ORD-Eintrag
ord-3074b2af783d43a49b22917efd9f1a18
Quelldatensatz
uspto-grants-1997_01
Patentnummer
US05593981

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