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

HRID 1420843
ノート
印刷プレビュー

反応式

HRID 1420843 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

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

生成物 1

HCID 187825851-Dimethylamino-4-(trifluoromethoxy)benzene収率 29.3%

試薬・触媒・溶媒 3

HCID 15049146(2-Methylphenyl)phosphane触媒HCID 962
Water
溶媒
HCID 1140Toluene溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-93bbbba332ef4812bb4992a04fb3d4fc
出典データセット
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06071927

反応ノート

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