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Triethylamine → 4-(1-Cyclobutyl piperidin-4-yloxy)benzonitrile

HRID 268719
ノート
印刷プレビュー

反応式

HRID 268719 の反応式
FC(F)(F)C(O)=O.[NH:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:22]=[CH:21][C:18]([C:19]#[N:20])=[CH:17][CH:16]=2)[CH2:10][CH2:9]1.C(N(CC)CC)C.[C:30]1(=O)[CH2:33][CH2:32][CH2:31]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl>[CH:30]1([N:8]2[CH2:9][CH2:10][CH:11]([O:14][C:15]3[CH:22]=[CH:21][C:18]([C:19]#[N:20])=[CH:17][CH:16]=3)[CH2:12][CH2:13]2)[CH2:33][CH2:32][CH2:31]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471TriethylamineHCID 14496CyclobutanoneHCID 5049666Sodium triacetoxyborohydrideHCID 179863194-(4-Piperidinyloxy)benzonitrile trifluoroacetate

生成物 1

HCID 98137774-(1-Cyclobutyl piperidin-4-yloxy)benzonitrile

試薬・触媒・溶媒 1

HCID 6344Dichloromethane
溶媒

実験手順

4-(4-Piperidinyloxy)benzonitrile trifluoroacetate (D22) (2.2 g) was dissolved in DCM (50 ml) and triethylamine (1.92 ml) was added followed by cyclobutanone (0.64 g). The mixture was stirred for 5 min, then sodium triacetoxyborohydride (1.94 g) was added and the reaction was stirred at rt under argon overnight. The reaction mixture was then washed with saturated potassium carbonate solution (3×30 ml) and brine (30 ml). The organic layer was dried (MgSO4) and evaporated to give the title compound (D23) as a white solid (1.91 g). 1H NMR δ (CDCl3): 7.56 (2H, d, J=6.84 Hz), 6.93 (2H, d, J=6.80 Hz), 4.41 (1H, m), 2.77 (1H, m), 2.75 (2H, m), 2.30 (2H, m), 2.06 (4H, m), 1.87 (4H, m), 1.66 (2H, m).

後処理

  1. stirringthe reaction was stirred at rt under argon overnight
  2. washThe reaction mixture was then washed with saturated potassium carbonate solution (3×30 ml) and brine (30 ml)
  3. dry with materialThe organic layer was dried (MgSO4)
  4. customevaporated

出典と根拠

ORDレコード
ord-1f68a7305cef4cfa92d31f331cd5747a
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07446103B2

反応ノート

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