Hydrochloric Acid → 2-Benzyl-7-methyl-2,3-dihydro-isoindol-1-one
反応式
[CH2:1]([N:8]1[C:16](=[O:17])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][C:14]=2[CH3:18])[C:9]1=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Sn].Cl.C(OCC)(=O)C>C(O)(C)C.CCCCCC>[CH2:1]([N:8]1[CH2:9][C:10]2[C:15](=[C:14]([CH3:18])[CH:13]=[CH:12][CH:11]=2)[C:16]1=[O:17])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
実験手順
A mixture of 2-benzyl-4-methyl-isoindole-1,3-dione (0.500 g, 2 mmol), tin (0.59 g, 5 mmol) and concentrated HCl (2 mL) in isopropanol (10 mL) was heated at reflux for 2.5 h. After this time, the reaction mixture was cooled to ambient temperature, the solids removed by filtration and the filtrate concentrated. The resulting material was dissolved in dichloromethane (20 mL) and the solution washed with brine (7 mL). The organic solution was separated, dried over anhydrous MgSO4, filtered, and concentrated to afford a mixture of regio isomers. Silica gel column chromatography of this mixture using 25% ethyl acetate in hexane afforded 2-benzyl-7-methyl-2,3-dihydro-isoindol-1-one (0.02 g, 9%); 1H NMR (300 MHz, CDCl3): δ ppm) 2.68 (s, 3H), 4.23 (s, 2H), 4.77 (s, 2H), 7.15-7.40 (m, 8H) and GC-MS: m/z 237 (M)+, 160 (M−77)+; and 2-benzyl-4-methyl-2,3-dihydro-isoindol-1-one (0.02 g, 9%); 1H NMR (300 MHz, CDCl3): δ (ppm) 2.68 (s, 3H), 4.23 (s, 2H), 4.77 (s, 2H), 7.15-7.40 (m, 8H) and GC-MS: m/z 237 (M)+, 160 (M−77)+.
後処理
- temperaturewas heated
- temperatureat reflux for 2.5 h
- customthe solids removed by filtration
- concentrationthe filtrate concentrated
- dissolutionThe resulting material was dissolved in dichloromethane (20 mL)
- washthe solution washed with brine (7 mL)
- customThe organic solution was separated
- dry with materialdried over anhydrous MgSO4
- filtrationfiltered
- concentrationconcentrated
- customto afford
- additiona mixture of regio isomers
出典と根拠
- ORDレコード
- ord-90aff08142e54a59aa64bd3a87088dec
- 出典データセット
- uspto-grants-2011_06
- 特許番号
- US07968570B2
反応ノート
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