Iodine → 17beta-Acetoxy-2-iodo-1alpha-methyl-androst-4-en-3-one

HRID 275070노트

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HRID 275070 반응식
[C:1]([O:4][C@H:5]1[CH2:10][CH2:9][C@H:8]2[C@H:11]3[C@H:21]([CH2:22][CH2:23][C@:6]12[CH3:7])[C@:19]1([CH3:20])[C:14](=[CH:15][C:16](=[O:25])[CH2:17][C@@H:18]1[CH3:24])[CH2:13][CH2:12]3)(=[O:3])[CH3:2].[I:26]I>C(O)(=O)C>[C:1]([O:4][C@H:5]1[CH2:10][CH2:9][C@H:8]2[C@H:11]3[C@H:21]([CH2:22][CH2:23][C@:6]12[CH3:7])[C@:19]1([CH3:20])[C:14](=[CH:15][C:16](=[O:25])[CH:17]([I:26])[C@@H:18]1[CH3:24])[CH2:13][CH2:12]3)(=[O:3])[CH3:2]

참가 물질

4

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온도
60 °C

실험 절차

6.88 g (20 mmol) of 17β-acetoxy-1α-methyl-androst-4-en-3-one and 1.75 g (22 mmol) of CuO in 60 ml of acetic acid are mixed with stirring at room temperature with 5.58 g (22 mmol) of iodine and stirred under nitrogen atmosphere for 24 hours at 60° C. Under reduced pressure, the acetic acid is largely distilled off and the residue is taken up in 100 ml of water. The water phase is extracted 3 times with 100 ml of ethyl acetate each. The ethyl acetate phases are washed with sodium thiosulfate solution and dried on sodium sulfate. After concentration by evaporation of the solution, 10 g of crude product is obtained. Recrystallization from ethyl acetate yields 8.8 g of 17β-acetoxy-2-iodo-1α-methyl-androst-4-en-3-one (93% of theory) of melting point 102° C.

후처리

  1. distillationUnder reduced pressure, the acetic acid is largely distilled off
  2. extractionThe water phase is extracted 3 times with 100 ml of ethyl acetate each
  3. washThe ethyl acetate phases are washed with sodium thiosulfate solution
  4. customdried on sodium sulfate
  5. concentrationAfter concentration
  6. customby evaporation of the solution
  7. custom10 g of crude product is obtained
  8. customRecrystallization from ethyl acetate

출처 및 근거

ORD 기록
ord-4888f098901b4f7f97854089f232c0f4
출처 데이터셋
uspto-grants-1995_02
특허 번호
US05391778

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