Ethyl Acetate → HCID 15307270、化合物

HRID 850829ノート

反応式

HRID 850829 の反応式
[F:1][CH:2](P(=O)(C1C=CC=CC=1)C1C=CC=CC=1)[F:3].[CH:18]([N-]C(C)C)([CH3:20])[CH3:19].[Li+].[CH3:26][O:27][C@H:28]1[CH2:45][C@@:43]2([CH3:44])[C@@H:39]([CH2:40][CH2:41][C:42]2=O)[C@H:38]2[C@H:29]1[C:30]1[CH:31]=[CH:32]C(OC3CCCCO3)=C[C:35]=1[CH2:36][CH2:37]2.[C:54]([O:57][CH2:58][CH3:59])(=[O:56])[CH3:55]>O1CCCC1.O>[F:1][C:2]([F:3])=[C:42]1[CH2:41][CH2:40][C@H:39]2[C@H:38]3[C@H:29]([C@@H:28]([O:27][CH3:26])[CH2:45][C@:43]12[CH3:44])[C:30]1[CH:31]=[CH:32][C:58]([O:57][CH:54]2[CH2:55][CH2:20][CH2:18][CH2:19][O:56]2)=[CH:59][C:35]=1[CH2:36][CH2:37]3

参加物

7

実験手順

A solution of 3 g of difluoromethyldiphenylphosphine oxide in 80 ml of tetrahydrofuran is slowly mixed with 5.85 ml of 2 M lithium diisopropylamide solution at a bath temperature of -50° C., and it is stirred for 1 hour. Then, a solution of 1.8 g of 11β-methoxy -3-tetrahydropyranyloxy-estra-1,3,5(10)-trien-17-one in 40 ml of tetrahydrofuran is slowly added, stirred for 15 minutes, slowly heated at a bath temperature of from -50° C. to 100° C. and refluxed for 2.5 hours. For working-up, it is diluted with ethyl acetate and water, suctioned off on Celite, rewashed with ethyl acetate, washed with water as well as with saturated sodium chloride solution, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/ethyl acetate/triethylamine. 1.3 g of 17-difluoromethylene-11β-methoxy-3-tetrahydropyranyloxy-estra -1,3,5(10)-triene is obtained with a melting point of 124-125° C., [α]D22 =+60.0° (c=0.505% in pyridine).

後処理

  1. stirringstirred for 15 minutes
  2. temperatureslowly heated at a bath temperature of from -50° C. to 100° C.
  3. temperaturerefluxed for 2.5 hours
  4. washwashed with water as well as with saturated sodium chloride solution
  5. customdried on sodium sulfate
  6. concentrationconcentrated by evaporation in a vacuum
  7. customchromatographed on silica gel with hexane/ethyl acetate/triethylamine

出典と根拠

ORDレコード
ord-ecabf467526a4b0d9c1060852369cfd2
出典データセット
uspto-grants-2000_01
特許番号
US06018062

反応ノート

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