tert-Butanol → Estra-4,16-dien-3-one

HRID 1107193Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1107193
C(O)(C)(C)C.[Li].[CH3:7][C@:8]12[CH2:24][CH2:23][C@H:22]3[C@@H:13]([CH2:14][CH2:15][C:16]4[CH:17]=[C:18]([OH:25])[CH:19]=[CH:20][C:21]=43)[C@@H:12]1[CH2:11][CH:10]=[CH:9]2>C1COCC1.N.CO>[CH3:7][C@:8]12[CH2:24][CH2:23][C@H:22]3[C@@H:13]([CH2:14][CH2:15][C:16]4[C@@H:21]3[CH2:20][CH2:19][C:18](=[O:25])[CH:17]=4)[C@@H:12]1[CH2:11][CH:10]=[CH:9]2

Komponenten

7

Edukt 3

HCID 6386tert-ButanolHCID 101988Estra-1,3,5(10),16-tetraen-3-olHCID 3028194Lithium

Produkt 1

HCID 15870982Estra-4,16-dien-3-one

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 222AmmoniaLösungsmittel2×HCID 887MethanolLösungsmittel2×HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To estra-1,3,5(10), 16-tetraene-3-methyl ether (551.5 mg., 2.055 mmol) in 8.6 ml of anhydrous THF, approximately 30 ml of anhydrous ammonia, and 6.76 g of t-butyl alcohol was added lithium wire (0.24 g, 35 mg-atom) cut in small pieces. The reaction mixture was refluxed 41/2 h under argon, after which methanol (2.3 ml) was added and the ammonia was allowed to boil off overnight. The residue was dissolved in 25 Ml of methanol and was acidified to approximately Ph 1 with 5N HCI. After heating in an oil bath between 55 and 70 C. for 15 min. the cooed hydrolysis mixture was partitioned between 25 ml of water and 50 ml of ethyl acetate and the aqueous phase was extracted with 25 ml of ethyl acetate. The combined organic extracts were washed with 25 ml of saturated sodium bicarbonate and 25 ml of brine, dried over magnesium sulfate, and filtered. Removal of solvent under reduced pressure yielded 0.57 g of oily residue which was purified by flash chromatography on silica gel (eluent: 15% ethyl acetate/hexane) followed by recrystallization from pentane to give crystals (206.1 mg, 39%) homogeneous to TLC, m.p. 67-71 C.

Aufarbeitung

  1. temperatureThe reaction mixture was refluxed 41/2 h under argon
  2. temperatureAfter heating in an oil bath between 55 and 70 C
  3. customfor 15 min. the cooed hydrolysis mixture
  4. customwas partitioned between 25 ml of water and 50 ml of ethyl acetate
  5. extractionthe aqueous phase was extracted with 25 ml of ethyl acetate
  6. washThe combined organic extracts were washed with 25 ml of saturated sodium bicarbonate and 25 ml of brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. customRemoval of solvent under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-d70f92d4429746519703c48e48a0c158
Quelldatensatz
uspto-grants-2000_05
Patentnummer
US06057439

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