Benzene → N-((1-(6-((2,6-Diisopropylphenylimino)methyl)pyridin-2-yl)naphthalen-2-yl)methyl)-2,4,6-trimethylaniline

HRID 2370668ノート

反応式

HRID 2370668 の反応式
C1C=CC=CC=1.[C:7]1([CH3:35])[CH:12]=[C:11]([CH3:13])[CH:10]=[C:9]([CH3:14])[C:8]=1[NH:15][CH2:16][C:17]1[CH:26]=[CH:25][C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:18]=1[C:27]1[N:32]=[C:31]([CH:33]=O)[CH:30]=[CH:29][CH:28]=1.[CH:36]([C:39]1[CH:45]=[CH:44][CH:43]=[C:42]([CH:46]([CH3:48])[CH3:47])[C:40]=1[NH2:41])([CH3:38])[CH3:37].O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CCOCC>[CH:46]([C:42]1[CH:43]=[CH:44][CH:45]=[C:39]([CH:36]([CH3:38])[CH3:37])[C:40]=1[N:41]=[CH:33][C:31]1[N:32]=[C:27]([C:18]2[C:19]3[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH:25]=[CH:26][C:17]=2[CH2:16][NH:15][C:8]2[C:7]([CH3:35])=[CH:12][C:11]([CH3:13])=[CH:10][C:9]=2[CH3:14])[CH:28]=[CH:29][CH:30]=1)([CH3:48])[CH3:47]

参加物

6

反応物 4

HCID 241BenzeneHCID 32484DiisopropylanilineHCID 521998p-Toluenesulfonic acid monohydrateHCID 866601036-{2-[(Mesitylamino)methyl]-1-naphthyl}pyridine-2-carbaldehyde

生成物 1

HCID 68003896N-((1-(6-((2,6-Diisopropylphenylimino)methyl)pyridin-2-yl)naphthalen-2-yl)methyl)-2,4,6-trimethylaniline

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
-20 °C

実験手順

Benzene (200 mL) was added to compound 5b (6.69 g, 17.6 mmol), and 2,6-diisopropylaniline (3.12 g, 17.6 mmol), and p-toluenesulfonic acid monohydrate (5 mg) in a 500 mL round-bottomed flask fitted with a Dean-Stark trap. The mixture was heated to reflux under nitrogen. After 2 hours, 1H NMR spectroscopy of an aliquot indicated that the reaction had proceeded to around 90% completion. All but about 50 mL of the benzene was removed by distillation and toluene (200 mL) was added. The mixture was heated to reflux and most of the toluene was removed by distillation. Drying of the residue under reduced pressure afforded a dirty yellow solid. Dissolution of the solid in warm Et2O, followed by filtration and cooling to −20° C. afforded 6b as nice yellow crystals. Yield from two crops: 6.5 g, 69%. 1H NMR (500 MHz, CD2Cl2): 8.36 (d, 1H), 8.33 (s, 1H), 7.97 (t, 1H), 7.93 (d, 2H), 7.59 (d, 1H), 7.39-7.51 (m, 4H), 7.17 (d, 2H), 7.10 (m, 1H), 6.72 (s, 2H), 4.01 (br d, 1H), 3.92 (d, 1H), 3.39 (br, 1H), 3.03 (sept, 2H), 2.18 (s, 3H), 2.03 (s, 6H), 1.18 (d, 12H).

後処理

  1. customfitted with a Dean-Stark trap
  2. temperatureThe mixture was heated
  3. temperatureto reflux under nitrogen
  4. customAll but about 50 mL of the benzene was removed by distillation and toluene (200 mL)
  5. additionwas added
  6. temperatureThe mixture was heated
  7. temperatureto reflux and most of the toluene
  8. customwas removed by distillation
  9. customDrying of the residue under reduced pressure
  10. customafforded a dirty yellow solid
  11. filtrationfollowed by filtration

出典と根拠

ORDレコード
ord-f12531b9a0f9446f89de5918fa80baf1
出典データセット
uspto-grants-2014_04
特許番号
US08710163B2

反応ノート

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