Ethanol → HCID 22282620, 화합물

HRID 2085338노트

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HRID 2085338 반응식
FC(S([C:8]1[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[S:11][CH2:10][CH:9]=1)(=O)=O)(F)F.[C:18]1([CH3:24])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.[Cl-].[Li+].[C:27](=O)([O-])[O-:28].[K+].[K+].C([OH:35])C>[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[S:11]1[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[C:8]([C:21]2[CH:22]=[CH:23][C:18]([C:24]([O:28][CH3:27])=[O:35])=[CH:19][CH:20]=2)=[CH:9][CH2:10]1

참가 물질

7

실험 절차

2H-1-benzothiopyran-4-yl trifluoromethyl sulfone from reaction 33a (1.83 g, 6.17 mmol) and 4-(methoxy carbonylphenyl)boronic acid (1.11 g, 6.17 mmol) were dissolved in ethanol (15 mL) and toluene (30 mL) under nitrogen at room temperature. Then lithium chloride (0.52 g, 12.35 mmol) and 2.65 M potassium carbonate (4.66 mL, 12.35 mmol) were added. Nitrogen was bubbled through the reaction for 15 minutes tetrakis(triphenylphosphine)-palladium(0) (0.35 g, 0.31 mmol) was added. The reaction was heated to reflux for 2 h, allowed to cool then partitioned between ethyl acetate and water. The organic layer was washed with water, brine, dried over magnesium sulfate, and was concentrated. The product was purified by chromatography on silica gel eluting with ethyl acetate:hexane (15:85, v:v) to give methyl 4-(2H-1-benzothiopyran-4-yl)benzoate (1.75 g, 67%) as a solid.

후처리

  1. customat room temperature
  2. additionwas added
  3. temperatureThe reaction was heated
  4. temperatureto reflux for 2 h
  5. temperatureto cool
  6. customthen partitioned between ethyl acetate and water
  7. washThe organic layer was washed with water, brine
  8. dry with materialdried over magnesium sulfate
  9. concentrationwas concentrated
  10. customThe product was purified by chromatography on silica gel eluting with ethyl acetate:hexane (15:85, v:v)

출처 및 근거

ORD 기록
ord-7a5350d4abc2474c95a7a221078cdaf4
출처 데이터셋
uspto-grants-2004_04
특허 번호
US06720329B2

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