1-Bromo-2-methylpropane → 4-(2-Methylpropoxy)benzonitrile

HRID 8047

反応式

HRID 8047 の反応式
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1)#[N:2].C(N(CC)CC)C.[CH2:17](Br)[CH:18]([CH3:20])[CH3:19]>CN(C=O)C.O>[CH2:17]([O:9][C:6]1[CH:7]=[CH:8][C:3]([C:1]#[N:2])=[CH:4][CH:5]=1)[CH:18]([CH3:20])[CH3:19]

参加物

6

反応物 3

HCID 65551-Bromo-2-methylpropaneHCID 8471TriethylamineHCID 130194-Cyanophenol

生成物 1

HCID 218937164-(2-Methylpropoxy)benzonitrile収率 85.6%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

To a solution of 4-cyanophenol (1.2 g, 10 mmol) in dry DMF (20 mL) was added triethylamine (20 mmol) followed by i-butyl bromide (2.7 g, 20 mmol). The resulting reaction mixture was stirred at 100° C. for 6 h. After cooling to room temperature, the reaction mixture was diluted with water (100 mL) and extracted with ethyl acetate (2×40 mL). The organic layer was washed with 4 M KOH (3×30 mL) and then with water, dried over Na2SO4 and concentrated under vacuum to provide 1.5 g (85%) 4-iso-butoxybenzo-nitrile that was used for the next step without further purification. 1H NMR (DMSO-D6): δ 0.95 (d, 6H, 2CH3), 2.0 (m, 1H, CH(CH3)2), 3.8 (d, 2H, CH2), 7.4 (AA′BB′, Δ=20 Hz, 4H, Ar).

後処理

  1. customThe resulting reaction mixture
  2. temperatureAfter cooling to room temperature
  3. extractionextracted with ethyl acetate (2×40 mL)
  4. washThe organic layer was washed with 4 M KOH (3×30 mL)
  5. dry with materialwith water, dried over Na2SO4
  6. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-178d1c80d262496d81b1b38dcd50183e
出典データセット
uspto-grants-2006_08
特許番号
US07087631B2

関連ノート

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