Nitromethane → 2-(3-(2-Nitro-ethyl)-phenyl)-pyridine

HRID 78044노트

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HRID 78044 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:8]=[C:9]([CH:12]=[CH:13][CH:14]=1)[CH:10]=O.[N+:15]([CH3:18])([O-:17])=[O:16].C([O-])(=O)C.[NH4+].[BH4-].[Na+]>O.C(O)(=O)C>[N+:15]([CH2:18][CH2:10][C:9]1[CH:8]=[C:7]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=2)[CH:14]=[CH:13][CH:12]=1)([O-:17])=[O:16]

참가 물질

7

반응물 4

HCID 6375NitromethaneHCID 517165Ammonium AcetateHCID 37100393-(Pyridin-2-yl)benzaldehydeHCID 4311764Sodium borohydride

생성물 1

HCID 592551612-(3-(2-Nitro-ethyl)-phenyl)-pyridine수율 71.2%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매2회

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온도
100 °C

실험 절차

To a mixture of 3-pyridin-2-yl-benzaldehyde (290 mg, 1.6 mmol) described in Manufacturing Example 84-1-1 and acetic acid (5 mL) were added nitromethane (0.65 mL, 12 mmol) and ammonium acetate (370 mg, 4.8 mmol), which was stirred for 2 hours at 100° C. The reaction mixture was cooled to room temperature and water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. A mixture of dimethyl sulfoxide (6 mL) and acetic acid (0.4 mL) was added to the resulting residue, and sodium borohydride (97 mg, 2.6 mmol) was added at room temperature while cooling appropriately. The reaction mixture was stirred for 10 minutes at the same temperature. Water was added to the reaction mixture at room temperature, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The resulting residue was purified by NH silica gel column chromatography (heptane:ethyl acetate=2:1) to obtain the title compound (260 mg, 71%).

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionfollowed by extraction with ethyl acetate
  3. washThe organic layer was washed with saturated aqueous sodium chloride
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customthe solvent was evaporated under a reduced pressure
  6. additionA mixture of dimethyl sulfoxide (6 mL) and acetic acid (0.4 mL)
  7. additionwas added at room temperature
  8. temperaturewhile cooling appropriately
  9. stirringThe reaction mixture was stirred for 10 minutes at the same temperature
  10. extractionwhich was then extracted with ethyl acetate
  11. washThe organic layer was washed with saturated aqueous sodium chloride
  12. concentrationwas concentrated under a reduced pressure
  13. customThe resulting residue was purified by NH silica gel column chromatography (heptane:ethyl acetate=2:1)

출처 및 근거

ORD 기록
ord-3809bb5a9f8c46d4b39ff2bcaaa24707
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08841327B2

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