2,2'-Bipyridine → (E)-4-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-enyl)-2-(trifluoromethoxy)benzoic acid

HRID 1502827ノート

反応式

HRID 1502827 の反応式
[F:1][C:2]([F:16])([F:15])[O:3][C:4]1[CH:12]=[C:11]([CH:13]=[CH2:14])[CH:10]=[CH:9][C:5]=1[C:6]([OH:8])=[O:7].Br[CH:18]([C:23]1[CH:28]=[C:27]([Cl:29])[C:26]([F:30])=[C:25]([Cl:31])[CH:24]=1)[C:19]([F:22])([F:21])[F:20].N1C=CC=CC=1C1C=CC=CN=1>CN1CCCC1.O.[Cu]Cl>[Cl:29][C:27]1[CH:28]=[C:23]([CH:18]([C:19]([F:22])([F:21])[F:20])/[CH:14]=[CH:13]/[C:11]2[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([O:3][C:2]([F:15])([F:16])[F:1])[CH:12]=2)[CH:24]=[C:25]([Cl:31])[C:26]=1[F:30]

参加物

7

反応物 3

HCID 14742,2'-BipyridineHCID 866751625-(1-Bromo-2,2,2-trifluoroethyl)-1,3-dichloro-2-fluorobenzeneHCID 893063732-(Trifluoromethoxy)-4-vinylbenzoic acid

生成物 1

HCID 86675151(E)-4-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-enyl)-2-(trifluoromethoxy)benzoic acid収率 41.1%

試薬・触媒・溶媒 3

HCID 62652Cuprous chloride触媒HCID 962Water溶媒HCID 84541-Methylpyrrolidine溶媒

反応条件

温度
150 °C

実験手順

To a stirred solution of 2-(trifluoromethoxy)-4-vinylbenzoic acid (0.356 g, 1.53 mmol) in 1N methylpyrrolidine (5.0 mL) was added 1-(1-bromo-2,2,2-trifluoroethyl)-3,5-dichloro 4-fluorobenzene (1.0 g, 3.07 mmol), copper(I) chloride (CuCl; 0.03 g, 0.307 mmol) and 2,2 bipyridyl (0.095 g, 0.614 mmol). The reaction mixture was stirred at 150° C. for 1 h. After the reaction was complete by TLC, the reaction mixture was diluted with water (100 mL) and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under reduced pressure to obtain the crude compound which was purified by flash column chromatography to afford the product as pale yellow gummy material (0.3 g, 21%): 1H NMR (400 MHz, CDCl3) δ 8.08 (d, J=8.0 Hz, 1H), 7.45 (d, J=1.6 Hz, 1H), 7.35 (s, 3H), 6.63 (d, J=16.0 Hz, 1H), 6.50 (dd, J=16.0, 8.0 Hz, 1H), 4.15 (m, 1H); ESIMS m/z 474.81 ([M−H]−).

後処理

  1. extractionextracted with ethyl acetate (2×50 mL)
  2. washThe combined organic layers were washed with brine
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated under reduced pressure
  5. customto obtain the crude compound which
  6. customwas purified by flash column chromatography

出典と根拠

ORDレコード
ord-114f086bd3774f26aed4a7d2345bb2b3
出典データセット
uspto-grants-2015_12
特許番号
US09211280B2

反応ノート

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