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

HRID 17168
ノート
印刷プレビュー

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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 728635-BromosalicylaldehydeHCID 76284hydroxylamine-O-sulfonic acidHCID 516892Sodium Bicarbonate

生成物 1

HCID 120030295-Bromo-1,2-benzoxazole

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒HCID 962Water溶媒
HCID 6344
Dichloromethane
溶媒

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
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07737160B2

反応ノート

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