反応式
[CH3:1][NH:2][CH2:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=[CH:6][CH:5]=1.C(N(CC)CC)C.[CH:21]([C:24]1[CH:31]=[CH:30][C:27]([CH2:28]Cl)=[CH:26][CH:25]=1)([CH3:23])[CH3:22]>O1CCCC1>[CH3:1][N:2]([CH2:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=[CH:6][CH:5]=1)[CH2:28][C:27]1[CH:30]=[CH:31][C:24]([CH:21]([CH3:23])[CH3:22])=[CH:25][CH:26]=1参加物
実験手順
1.71 g (0.01 mole) of N-methyl-1-naphthylmethylamine was dissolved in 30 ml of tetrahydrofuran, and 1.2 g (0.012 mole) of triethylamine was added. With stirring at room temperature, 1.85 g (0.011 mole) of p-isopropylbenzyl chloride was added, and the mixture was reacted at room temperature for 6 hours. The reaction mixture was filtered, and the solvent was removed under reduced pressure. The residue was distributed between ether and a saturated aqueous solution of sodium hydrogen carbonate, and the organic layer was collected. The organic layer was washed with water, dried over sodium sulfate and then concentrated under reduced pressure. The residue was chromatographed on a silica gel column and eluted with 4% ethyl acetate/n-hexane. The eluate was concentrated to give 2.82 g (yield 93%) of an oily substance.
後処理
- customthe mixture was reacted at room temperature for 6 hours
- filtrationThe reaction mixture was filtered
- customthe solvent was removed under reduced pressure
- customa saturated aqueous solution of sodium hydrogen carbonate, and the organic layer was collected
- washThe organic layer was washed with water
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was chromatographed on a silica gel column
- washeluted with 4% ethyl acetate/n-hexane
- concentrationThe eluate was concentrated
- customto give 2.82 g (yield 93%) of an oily substance
出典と根拠
- ORDレコード
- ord-f0cb3401965b4b0a9c91437b251e1b78
- 出典データセット
- uspto-grants-1989_04
- 特許番号
- US04822822
関連ノート
読み込み中…