Ammonia → 3-Methoxyestra-2,5(10)-dien-17beta-ol

HRID 1077214

反応式

HRID 1077214 の反応式
[CH3:1][O:2][C:3]1[CH:20]=[CH:19][C:18]2[C@@H:17]3[C@H:8]([C@H:9]4[C@@:13]([CH2:15][CH2:16]3)([CH3:14])[C@@H:12]([OH:21])[CH2:11][CH2:10]4)[CH2:7][CH2:6][C:5]=2[CH:4]=1.[Li].N.[Cl-].[NH4+]>O1CCCC1.O.C(O)C>[CH3:1][O:2][C:3]1[CH2:4][C:5]2[CH2:6][CH2:7][C@@H:8]3[C@@H:17]([C:18]=2[CH2:19][CH:20]=1)[CH2:16][CH2:15][C@@:13]1([CH3:14])[C@H:9]3[CH2:10][CH2:11][C@@H:12]1[OH:21]

参加物

8

反応物 4

HCID 222AmmoniaHCID 25517Ammonium ChlorideHCID 246206Estradiol 3-methyl etherHCID 3028194Lithium

生成物 1

HCID 1019633-Methoxyestra-2,5(10)-dien-17beta-ol収率 64.2%

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

Add dl-3-methoxyestra-1,3,5(10)-trien-17β-ol (1.3 g) in tetrahydrofuran (40 ml) to a stirred solution of lithium (1.3 g) in liquid ammonia (100 ml). After 15 minutes add ethanol (20 ml) dropwise and when the blue color is discharged add ammonium chloride and water and extract the mixture with ether. Wash, dry and evaporate the ethereal solution and recrystallize the residue from ethanol-hexane to obtain dl-3-methoxyestra-2,5(10)-dien-17β-ol (0.84 g), m.p. 120-123°; infrared absorption maxima at 3.25 μ, 5.8 μ, 6 μ.

後処理

  1. extractionextract the mixture with ether
  2. washWash
  3. customdry
  4. customevaporate the ethereal solution
  5. customrecrystallize the residue from ethanol-hexane

出典と根拠

ORDレコード
ord-f388ce3e178d4d83ac4255bc30913c7e
出典データセット
uspto-grants-1976_05
特許番号
US03959322

関連ノート

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