1-Bromo-3-chlorobenzene → 3-Bromo-5-chlorophenol

HRID 60658

반응식

HRID 60658 반응식
B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)[O:2]1.[Br:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([Cl:26])[CH:21]=1.OOS([O-])=O.[K+]>O.C(Cl)Cl.C[OH2+].C[OH2+].C1CC=CCCC=C1.C1CC=CCCC=C1.[Ir].[Ir]>[Br:19][C:20]1[CH:25]=[C:24]([OH:2])[CH:23]=[C:22]([Cl:26])[CH:21]=1

참가 물질

7

실험 절차

A flask containing (1,5-cyclooctadiene)(methoxy)-iridium(I) dimer (84 mg, 0.13 mmol), 4,4′-di-tert butyl-2-2′-dipyridyl (69 mg, 0.26 mmol) and bis(pinacolato)diboron (1.29 g, 5.11 mmol) was purged with Ar, then hexanes (26 mL) and 1-bromo-3-chlorobenzene (1 mL, 8.51 mmol) were added sequentially. The solution was stirred at RT for 18 h. The reaction mixture was concentrated in vacuo, re-dissolved in acetone (26 mL), then oxone (5.23 g, 8.51 mmol) in water (26 mL) added [Caution: exotherm observed]. After 10 min, the reaction mixture was diluted with DCM. The layers separated, and the aqueous layer extracted with DCM. The combined organics were washed with brine, dried and concentrated in vacuo to give the title compound (1.43 g, 81%). LCMS (Method 3): Rt 3.74 min, m/z 205, 207 [M-H+].

후처리

  1. customwas purged with Ar
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. dissolutionre-dissolved in acetone (26 mL)
  4. waitAfter 10 min
  5. customThe layers separated
  6. extractionthe aqueous layer extracted with DCM
  7. washThe combined organics were washed with brine
  8. customdried
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-e7b420fca4cd44b99f56ad6c52a98cc7
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09440974B2

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