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2,2'-Bipyridine → (E)-ethyl 4-(3-(3,5-dichlorophenyl)-4,4,4-trifluorobut-1-enyl)-2-methylbenzoate

HRID 587667
ノート
印刷プレビュー

反応式

HRID 587667 の反応式
[CH3:1][C:2]1[CH:12]=[C:11]([CH:13]=[CH2:14])[CH:10]=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5].Br[CH:16]([C:21]1[CH:26]=[C:25]([Cl:27])[CH:24]=[C:23]([Cl:28])[CH:22]=1)[C:17]([F:20])([F:19])[F:18].N1C=CC=CC=1C1C=CC=CN=1>ClC1C=CC=CC=1Cl.Cl[Cu]>[Cl:27][C:25]1[CH:26]=[C:21]([CH:16]([C:17]([F:20])([F:18])[F:19])/[CH:14]=[CH:13]/[C:11]2[CH:10]=[CH:9][C:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])=[C:2]([CH3:1])[CH:12]=2)[CH:22]=[C:23]([Cl:28])[CH:24]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 14742,2'-BipyridineHCID 58390837Ethyl 2-methyl-4-vinylbenzoateHCID 866751181-(1-Bromo-2,2,2-trifluoroethyl)-3,5-dichlorobenzene

生成物 1

HCID 86675123(E)-ethyl 4-(3-(3,5-dichlorophenyl)-4,4,4-trifluorobut-1-enyl)-2-methylbenzoate収率 40%

試薬・触媒・溶媒 2

HCID 62652Cuprous chloride触媒
HCID 7239
1,2-Dichlorobenzene
溶媒

反応条件

温度
180 °C

実験手順

To a stirred solution of ethyl 2-methyl-4-vinylbenzoate (2.0 g, 10.5 mmol) in 1,2-dichlorobenzene (25 mL) were added 1-(1-bromo-2,2,2-trifluoroethyl)-3,5-dichlorobenzene (6.44 g, 21.0 mmol), CuCl (208 mg, 21 mmol) and 2,2bipyridyl (0.65 g, 4.1 mmol). The reaction mixture was degassed with argon for 30 min and then stirred at 180° C. for 24 h. After the reaction was deemed complete by TLC, the reaction mixture was cooled to 25° C. and filtered, and the filtrate was concentrated under reduced pressure. Purification by flash chromatography (SiO2, 100-200 mesh; eluting with 25-30% EtOAc in petroleum ether) afforded the title compound as a solid (1.7 g, 40%): 1H NMR (400 MHz, CDCl3) δ 7.91 (d, J =8.0 Hz, 1H), 7.37 (m, 1H), 7.27-7.24 (m, 4H), 6.59 (d, J=16.0 Hz, 1H), 6.59 (dd, J=16.0, 8.0 Hz, 1H), 4.38 (q, J=7.2 Hz, 2H), 4.08 (m, 1H), 2.62 (s, 3H), 1.42 (t, J=7.2 Hz, 3H); ESIMS m/z 415.06 ([M−H]−); IR (thin film) 1717, 1255, 1114 cm−1.

後処理

  1. customThe reaction mixture was degassed with argon for 30 min
  2. temperaturethe reaction mixture was cooled to 25° C.
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customPurification
  6. washby flash chromatography (SiO2, 100-200 mesh; eluting with 25-30% EtOAc in petroleum ether)

出典と根拠

ORDレコード
ord-24131f4e87ea477888061b2f017277e4
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09226501B2

反応ノート

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