tert-Butanol → Estra-4,16-dien-3-one

HRID 1108452노트

반응식

HRID 1108452 반응식
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

참가 물질

7

반응물 3

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

생성물 1

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

시약·촉매·용매 3

HCID 222Ammonia용매2회HCID 887Methanol용매2회HCID 8028Tetrahydrofuran용매

실험 절차

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 4 1/2 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.

후처리

  1. temperatureThe reaction mixture was refluxed 4 1/2 h under argon
  2. temperatureAfter heating in an oil bath between 55 and 70 C for 15 min.
  3. customthe 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

출처 및 근거

ORD 기록
ord-ad22772e2c5a421aaa1dd6b71c199908
출처 데이터셋
uspto-grants-2000_05
특허 번호
US06066627

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