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Acetic Acid → HCID 70501935, Verbindung

HRID 543652
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 543652
[I:1]I.I([O-])(=O)=O.[K+].[CH3:8][C:9]1[CH2:10][C@H:11]2[C@:24]([CH3:27])([CH2:25][CH:26]=1)[C@@H:23]1[C@H:14]([C@H:15]3[C@@:19]([CH2:21][CH2:22]1)([CH3:20])[C:18](=[O:28])[CH2:17][CH2:16]3)[CH2:13][CH2:12]2.O.[C:30]([OH:33])(=[O:32])[CH3:31]>>[C:30]([O:33][C@H:26]1[CH2:25][C@@:24]2([CH3:27])[C@@H:11]([CH2:12][CH2:13][C@@H:14]3[C@@H:23]2[CH2:22][CH2:21][C@@:19]2([CH3:20])[C@H:15]3[CH2:16][CH2:17][C:18]2=[O:28])[CH2:10][C@@:9]1([I:1])[CH3:8])(=[O:32])[CH3:31]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 176Acetic AcidHCID 807IodineHCID 962WaterHCID 23665710Potassium IodateHCID 68866327HCID 68866327, Verbindung

Produkt 1

HCID 70501935HCID 70501935, Verbindung

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

Iodine (47 g) and potassium iodate (18 g) were added to a solution of 3-methyl-5α-androst-2-en-17-one (100 g) in glacial acetic acid (3 l) and the mixture was stirred at 60° C. for 1.5 h. The mixture was cooled to room temperature, water (2.5 l) was added and the product was extracted into diethyl ether. The extract was washed with potassium bicarbonate solution (1 l), sodium sulphite solution (500 ml) and finally with water (3×1 l) to neutrality. The organic layer was dried (MgSO4) and concentrated to yield 2β-acetyloxy-3α-iodo-3β-methyl-5α-androstan-17-one as a colourless solid (94.03 g).

Aufarbeitung

  1. temperatureThe mixture was cooled to room temperature
  2. extractionthe product was extracted into diethyl ether
  3. washThe extract was washed with potassium bicarbonate solution (1 l), sodium sulphite solution (500 ml) and finally with water (3×1 l) to neutrality
  4. dry with materialThe organic layer was dried (MgSO4)
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-299ec95641f3455ea70704ee9e99b8c6
Quelldatensatz
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04447425

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