Sodium Carbonate → 4'-Chloro-2'-methyl-[1,1'-biphenyl]-4-amine

HRID 1401880노트

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HRID 1401880 반응식
I[C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.[CH3:9][C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=1B(O)O.C([O-])([O-])=O.[Na+].[Na+]>COCCOC.CCO.O>[Cl:16][C:14]1[CH:13]=[CH:12][C:11]([C:2]2[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=2)=[C:10]([CH3:9])[CH:15]=1

참가 물질

5

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온도
125 °C

실험 절차

A mixture of 4-iodo-aniline (25.0 g, 114.1 mmol), 2-methyl-4-chlorophenyl-boronic acid (29.17 g, 171.1 mmol), PdCl2(P(o-tolyl)3)2 (11.66 g, 14.8 mmol), and Na2CO3 (60.49 g, 570.7 mmol) in DME/EtOH/H2O (100/50/25 mL) was heated 125° C. for 2 h. The reaction mixture was cooled to room temperature, filtered and washed with EtOAc (200 mL). The solvent was removed under reduced pressure. The crude mixture was extracted with ethyl acetate (500 mL) and the organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The resulting crude was purified by column chromatography on silica gel, eluting with 5-30% Hexane/EtOAc to afford 4′-Chloro-2′-methyl biphenyl-4-ylamine. 1H NMR (300 MHz, CDCl3): δ 7.24-7.08 (m, 5 H), 6.72 (d. J=7.2 Hz, 2 H), 3.70 (bs, 2 H), 2.27 (s, 3 H).

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationfiltered
  3. washwashed with EtOAc (200 mL)
  4. customThe solvent was removed under reduced pressure
  5. extractionThe crude mixture was extracted with ethyl acetate (500 mL)
  6. washthe organic layer was washed with brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated under reduced pressure
  9. customThe resulting crude was purified by column chromatography on silica gel
  10. washeluting with 5-30% Hexane/EtOAc

출처 및 근거

ORD 기록
ord-a6ab28a8dce341ad8d9760561ccdfb65
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08907103B2

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