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3,5-Dibromosalicylaldehyde → 6,8-dibromo-2H-chromen-2-one

HRID 841868
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HRID 841868 반응식
[Br:1][C:2]1[CH:9]=[C:8]([Br:10])[CH:7]=[C:4]([CH:5]=O)[C:3]=1[OH:11].[C:12](OC(=O)C)(=[O:14])[CH3:13].C(N(CC)CC)C>>[Br:10][C:8]1[CH:7]=[C:4]2[C:3](=[C:2]([Br:1])[CH:9]=1)[O:11][C:12](=[O:14])[CH:13]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 70243,5-DibromosalicylaldehydeHCID 7918Acetic AnhydrideHCID 8471Triethylamine

생성물 1

HCID 217668716,8-dibromo-2H-chromen-2-one수율 87%

실험 절차

To a suspension of 3,5-dibromosalicylaldehyde (100 g, 357 mmol) in acetic anhydride (164.8 mL, 1.8 mol) was added triethylamine (45 mL, 375 mmol). The reaction solution was heated overnight at reflux under argon. The solution was cooled to room temperature and a solid mass formed. The dark brown reaction mixture was washed with hot hexanes (3×300 mL) and aqueous saturated sodium bicarbonate. The resulting solid was dissolved in EtOAc (2 L) and washed with water. The organic layer was dried (sodium sulfate) and concentrated to give a brown solid that was collected by filtration. The solid was dried in vacuo to give substantially pure 6,8-dibromocoumarin (94.2 g, 87% yield).

후처리

  1. temperatureThe reaction solution was heated overnight
  2. temperatureat reflux under argon
  3. customa solid mass formed
  4. washThe dark brown reaction mixture was washed with hot hexanes (3×300 mL) and aqueous saturated sodium bicarbonate
  5. dissolutionThe resulting solid was dissolved in EtOAc (2 L)
  6. washwashed with water
  7. dry with materialThe organic layer was dried (sodium sulfate)
  8. concentrationconcentrated
  9. customto give a brown solid
  10. filtrationthat was collected by filtration
  11. customThe solid was dried in vacuo

출처 및 근거

ORD 기록
ord-4968485cc85145928b5f9680ad0113ce
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06372719B1

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