Potassium Phosphate, Tribasic → 4-Chloro-2-cyclopropyl-benzaldehyde

HRID 1748736노트

반응식

HRID 1748736 반응식
[CH:1]1([B-](F)(F)F)[CH2:3][CH2:2]1.[K+].P([O-])([O-])([O-])=O.[K+].[K+].[K+].Br[C:18]1[CH:25]=[C:24]([Cl:26])[CH:23]=[CH:22][C:19]=1[CH:20]=[O:21].C1(P(C2CCCCC2)C2C=CC=CC=2C2C(OC(C)C)=CC=CC=2OC(C)C)CCCCC1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C(OCC)(=O)C.O.C1(C)C=CC=CC=1>[Cl:26][C:24]1[CH:23]=[CH:22][C:19]([CH:20]=[O:21])=[C:18]([CH:1]2[CH2:3][CH2:2]2)[CH:25]=1

참가 물질

9

실험 절차

To a degassed mixture of toluene (60 mL) and water (9 mL) was added potassium cyclopropyl-trifluoroborate (0.91 g, 6.2 mmol) and tribasic potassium phosphate (6.37 g, 30 mmol). The resulting mixture was stirred for 15 min at rt, thereafter, 2-bromo-4-chlorobenzaldehyde (1.50 g, 6.84 mmol, WO2006044454), palladium(II) acetate (0.11 g, 0.5 mmol) and 2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl (0.48 g, 1.0 mmol) were added and the mixture was heated under reflux, overnight. After cooling to rt, water (50 mL) and ethyl acetate (50 mL) were added and the layers were separated. The organic layer was washed with brine (20 mL), dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (SiO2, DCM/hexanes 1:3) to give 4-chloro-2-cyclopropyl-benzaldehyde (0.48 g, 2.6 mmol, 39%) as a colorless semi solid: 1H-NMR (CDCl3, Bruker 400 MHz) δ 0.80 (2 H, m), 1.08-1.17 (2 H, m), 2.58 (1 H, m), 7.10 (1 H, d, J=2 Hz), 7.29 (1 H, dd, J=8 Hz, 2 Hz), 7.75 (1 H, d, J=8 Hz), 10.6 (1 H, s).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux, overnight
  3. temperatureAfter cooling to rt
  4. customthe layers were separated
  5. washThe organic layer was washed with brine (20 mL)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by column chromatography (SiO2, DCM/hexanes 1:3)

출처 및 근거

ORD 기록
ord-912ba6cacb634541b1c015fc7b546a0e
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09150592B2

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