N-Methylbenzylamine → N-methyl-1-phenyl-N-[(2,4,6,7-tetramethyl-2,3-dihydro-1-benzofuran-2-yl)methyl]methanamine

HRID 1850415ノート

反応式

HRID 1850415 の反応式
[CH3:1][NH:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.C(=O)([O-])[O-].[K+].[K+].CC(N(C)C)=O.I[CH2:23][C:24]1([CH3:36])[CH2:28][C:27]2[C:29]([CH3:35])=[CH:30][C:31]([CH3:34])=[C:32]([CH3:33])[C:26]=2[O:25]1>C(OCC)(=O)C.O>[CH3:1][N:2]([CH2:23][C:24]1([CH3:36])[CH2:28][C:27]2[C:29]([CH3:35])=[CH:30][C:31]([CH3:34])=[C:32]([CH3:33])[C:26]=2[O:25]1)[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1

参加物

7

実験手順

N-methylbenzylamine (766 mg, 3.16 mmol) and potassium carbonate (1.09 g, 7.90 mmol) were added to a solution of DMA (5 mL) containing 2-(iodomethyl)-2,4,6,7-tetramethyl-2,3-dihydro-1-benzofuran (1.00 g, 3.16 mmol) synthesized in Reference Example 126, and the mixture was stirred under heated reflux for 4 hours. The reaction solution was cooled to room temperature, and water and ethyl acetate were added thereto to separate an organic layer. The organic layer was washed with water and saturated saline, and dried using anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was purified by silica gel chromatography (hexane-ethyl acetate 99:1-93:7) to give 730 mg of the title compound (yield: 75%).

後処理

  1. customsynthesized in Reference Example 126
  2. temperatureunder heated
  3. temperaturereflux for 4 hours
  4. customto separate an organic layer
  5. washThe organic layer was washed with water and saturated saline
  6. customdried
  7. concentrationfollowed by concentration under reduced pressure
  8. customThe residue was purified by silica gel chromatography (hexane-ethyl acetate 99:1-93:7)

出典と根拠

ORDレコード
ord-94c7227b0cfe43b0b6be8e438af43af6
出典データセット
uspto-grants-2015_02
特許番号
US08957069B2

反応ノート

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