5-Bromosalicylaldehyde → 5-Bromo-1,2-benzoxazole

HRID 17168

反応式

HRID 17168 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:10])=[C:6]([CH:9]=1)[CH:7]=O.[NH2:11]OS(O)(=O)=O.C(=O)(O)[O-].[Na+]>C(O)C.ClCCl.O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][N:11]=[CH:7][C:6]=2[CH:9]=1

参加物

7

反応条件

温度
0 °C

実験手順

A solution of 5-bromo-2-hydroxy-benzaldehyde (2.0 g, 10 mmol) in ethanol (10 mL) at room temperature was treated with hydroxylamine-O-sulfonic acid (1.69 g, 15 mmol), stirred for 20 minutes, diluted with dichloromethane (50 mL), cooled to 0° C. and treated with a solution of sodium bicarbonate (3 g) in water (25 mL). The solution was stirred at 0° C. for 30 minutes. The organic layer was removed and the aqueous layer was extracted with dichloromethane. The aqueous layer was treated with additional dichloromethane (50 mL) and stirring was continued for one hour. The layers were separated and the aqueous layer was extracted with dicloromethane. The combined organic layers were washed with brine, dried (MgSO4) and concentrated. The concentrate was recrystallized from ethanol to give 970 mg (49%) yield of the desired product. MS (ESI(−)) m/e 195.9, 197.9 (M−H)−

後処理

  1. stirringThe solution was stirred at 0° C. for 30 minutes
  2. customThe organic layer was removed
  3. extractionthe aqueous layer was extracted with dichloromethane
  4. additionThe aqueous layer was treated with additional dichloromethane (50 mL)
  5. stirringstirring
  6. waitwas continued for one hour
  7. customThe layers were separated
  8. extractionthe aqueous layer was extracted with dicloromethane
  9. washThe combined organic layers were washed with brine
  10. dry with materialdried (MgSO4)
  11. concentrationconcentrated
  12. customThe concentrate was recrystallized from ethanol

出典と根拠

ORDレコード
ord-d2a564846363457bbd5a6780f7989129
出典データセット
uspto-grants-2010_06
特許番号
US07737160B2

関連ノート

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