Sodium Carbonate → 2-(3-Methoxyphenyl)-6,7-dihydro-5H-benzo[b]thiophen-4-one

HRID 2063746노트

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HRID 2063746 반응식
Br[C:2]1[S:6][C:5]2[CH2:7][CH2:8][CH2:9][C:10](=[O:11])[C:4]=2[CH:3]=1.B(O)O.[CH3:15][O:16][C:17]1[CH:18]=[C:19](O)[CH:20]=[CH:21][CH:22]=1.C([O-])([O-])=O.[Na+].[Na+].CCO.O>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.COCCOC>[CH3:15][O:16][C:17]1[CH:22]=[C:21]([C:2]2[S:6][C:5]3[CH2:7][CH2:8][CH2:9][C:10](=[O:11])[C:4]=3[CH:3]=2)[CH:20]=[CH:19][CH:18]=1

참가 물질

7

실험 절차

To 2-bromo-6,7-dihydro-5H-benzo[b]thiophen-4-one (5 g, 21.74 mmol) was successively added 3-methoxyphenol boronic acid (3.63 g, 23.92 mmol), 2M Na2CO3(aq) (43.5 mL, 86.98 mmol), Pd(PPh3)4 (251 mg, 0.22 mmol), 3:4 EtOH/H2O (37.5 mL) and DME (62.5 mL). The reaction mixture was degassed and heated to reflux for 12 hours. EtOAc (250 mL) was added and the crude reaction mixture was washed with water (2×100 mL). The organic layer was dried over magnesium sulphate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with EtOAc:hexanes (20:80) to give the title compound as an off-white solid in 95% yield. MS (ES+) 259. δH (d6 DMSO) 2.13 (2H, quint.), 2.50 (2H, m), 3.05 (2H, t), 3.81 (3H, s), 6.91 (1H, m), 7.20-7.22 (2H, m), 7.34 (1H, m), 7.67 (1H, s).

후처리

  1. customThe reaction mixture was degassed
  2. temperatureheated
  3. temperatureto reflux for 12 hours
  4. additionEtOAc (250 mL) was added
  5. customthe crude reaction mixture
  6. washwas washed with water (2×100 mL)
  7. dry with materialThe organic layer was dried over magnesium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified by silica gel chromatography
  11. washeluting with EtOAc:hexanes (20:80)

출처 및 근거

ORD 기록
ord-4bf61ec677af46e78cc65ca38e0e4ccb
출처 데이터셋
uspto-grants-2012_10
특허 번호
US08288400B2

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