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Potassium Carbonate → 3-Bromo-2-methyl-1-benzofuran

HRID 2181682
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HRID 2181682 반응식
O1[C:5]2[CH:6]=[CH:7][C:8]([C:10](OC)=O)=C[C:4]=2[CH:3]=[CH:2]1.[C:14]([O-:17])(O)=O.[Na+].[Br:19]Br.C([O-])([O-])=O.[K+].[K+]>C(Cl)Cl>[CH3:10][C:8]1[O:17][C:14]2[CH:2]=[CH:3][CH:4]=[CH:5][C:6]=2[C:7]=1[Br:19]
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참가 물질

6

반응물 4

HCID 11430Potassium CarbonateHCID 24408BromineHCID 516892Sodium BicarbonateHCID 12674941Methyl 1-benzofuran-5-carboxylate

생성물 1

HCID 115140063-Bromo-2-methyl-1-benzofuran수율 75%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Methyl benzofuran-5-carboxylate (1.74 g, 9.9 mmol) is dissolved in CH2Cl2 (50 mL), layered with saturated NaHCO3 (75 mL) using very slow magnetic stirring so that the two layers are not mixed and treated with Br2 (3.1 mL, 59.1 mmol). The bi-phasic mixture is stirred slowly for 2 h, then vigorously for 1 h. The layers are separated and the aqueous layer is extracted with CH2Cl2 (2×50 mL). The organics are dried (Na2SO4) and concentrated under reduced pressure without heat. The residue is dissolved in MeOH (100 mL), treated with K2CO3 (8.17 g, 59.1 mmol) and stirred at RT for 18 h. The mixture is concentrated to dryness, partitioned between 50% saturated NaHCO3 (75 mL) and EtOAc (2×75 mL) and the organics are dried (Na2SO4) and concentrated in vacuo. The crude material (2.21 g) is adsorbed onto silica gel (4.5 g) chromatographed over 90 g slurry-packed silica gel, eluting with 8% EtOAc/hexane then 15% EtOAc/hexane. The appropriate fractions are combined and concentrated to afford 1.88 g (75%) of methyl 3-bromo-1-benzofuran as a white solid. 1H NMR (300 MHz, CDCl3): δ 3.99, 7.55, 7.74, 8.11, 8.31 ppm.

후처리

  1. additionare not mixed
  2. stirringThe bi-phasic mixture is stirred slowly for 2 h
  3. customThe layers are separated
  4. extractionthe aqueous layer is extracted with CH2Cl2 (2×50 mL)
  5. dry with materialThe organics are dried (Na2SO4)
  6. concentrationconcentrated under reduced pressure
  7. temperaturewithout heat
  8. dissolutionThe residue is dissolved in MeOH (100 mL)
  9. stirringstirred at RT for 18 h
  10. concentrationThe mixture is concentrated to dryness
  11. custompartitioned between 50% saturated NaHCO3 (75 mL) and EtOAc (2×75 mL)
  12. dry with materialthe organics are dried (Na2SO4)
  13. concentrationconcentrated in vacuo
  14. customchromatographed over 90 g slurry-packed silica gel
  15. washeluting with 8% EtOAc/hexane
  16. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a9816272ace9401084383231913760ad
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06894042B2

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