Hydrogen Peroxide → 查耳酮ALPHA环氧化物

HRID 259431

反应方程式

HRID 259431 反应方程式
[CH:1](=[CH:8][C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH:17]O.[OH-].[Na+]>CO>[C:2]1([C:1](=[O:17])[CH:8]2[O:10][CH:9]2[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参与物

5

反应物 3

HCID 784Hydrogen PeroxideHCID 7189查耳酮HCID 14798二甲基对苯二胺二盐酸

产物 1

HCID 92219查耳酮ALPHA环氧化物

试剂、催化剂与溶剂 1

HCID 887(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮溶剂

实验过程

To a mechanically stirred mixture of 83.2 g benzalacetophenone (0.3m), 1000 ml methanol and 120 ml 15% hydrogen peroxide was added 100 ml 2N sodium hydroxide solution, while maintaining the temperature below 30° by external cooling. After completed addition, the mixture was left standing at room temperature for 20 min. The crystalline precipitate was filtered off, washed with water and recrystallized from methanol. There were obtained 59.6 g 1,3-diphenyl-2,3-epoxy-1-propanone; m.p. 90° C.

后处理

  1. temperaturewhile maintaining the temperature below 30° by external cooling
  2. additionaddition
  3. waitthe mixture was left
  4. filtrationThe crystalline precipitate was filtered off
  5. washwashed with water
  6. customrecrystallized from methanol

来源与证据

ORD记录
ord-81b9796c644749a9b95c4d65aec2b733
来源数据集
uspto-grants-1977_07
专利号
US04038289

关联笔记

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