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Tris(dimethylamino)borane → 1-Dimethylamino-4-(trifluoromethoxy)benzene

HRID 1420843
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HRID 1420843 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]([F:12])([F:11])[F:10])=[CH:4][CH:3]=1.[CH3:13][N:14](B(N(C)C)N(C)C)[CH3:15].CC(C)([O-])C.[Na+]>C1(C)C=CC=CC=1.O.C1(C)C=CC=CC=1P>[CH3:13][N:14]([CH3:15])[C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]([F:12])([F:11])[F:10])=[CH:4][CH:3]=1
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참가 물질

7

반응물 3

HCID 78081Tris(dimethylamino)boraneHCID 5210081-Bromo-4-(trifluoromethoxy)benzeneHCID 23676156Sodium t-butoxide

생성물 1

HCID 187825851-Dimethylamino-4-(trifluoromethoxy)benzene수율 29.3%

시약·촉매·용매 3

HCID 15049146(2-Methylphenyl)phosphane촉매HCID 962
Water
용매
HCID 1140Toluene용매

실험 절차

A mixture of 1-bromo-4-(trifluoromethoxy)benzene (2.41 g), tris(dimethylamino)borane (1.43 g), sodium t-butoxide (1.34 g), tris(dibenzylideneacetone)dipallidium (18 mg), and o-tolylphosphine (12 mg) in toluene (30 ml) was heated under reflux for 4 h. The mixture was cooled, diluted with water (30 mL) and extracted with ethyl acetate (3×10 mL). The combined organic fractions were washed with brine, dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by chromatography on silica gel, eluting with hexane/EtOAc (99:1 increasing to (95:5) to give the title compound as an oil (600 mg). 1H NMR (360 MHz, CDCl3) δ2.95 (6 H, s), 6.66 (2 H, d, J 9 Hz), and 7.08 (2 H, d, J 8.5 Hz). m/z (ES+) m/z 206 (M+1).

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 4 h
  3. temperatureThe mixture was cooled
  4. extractionextracted with ethyl acetate (3×10 mL)
  5. washThe combined organic fractions were washed with brine
  6. dry with materialdried (MgSO4)
  7. customthe solvent was evaporated under reduced pressure
  8. customThe residue was purified by chromatography on silica gel
  9. washeluting with hexane/EtOAc (99:1 increasing to (95:5)

출처 및 근거

ORD 기록
ord-93bbbba332ef4812bb4992a04fb3d4fc
출처 데이터셋
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06071927

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