Diethyl Ether → Dibenzyl 5-aminoisophthalate
反応式
[CH2:1]([O:8][C:9](=[O:29])[C:10]1[CH:25]=[C:24]([N+:26]([O-])=O)[CH:23]=[C:12]([C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:14])[CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CCOCC>C(O)(=O)C.[Zn]>[CH2:16]([O:15][C:13](=[O:14])[C:12]1[CH:23]=[C:24]([NH2:26])[CH:25]=[C:10]([C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[O:29])[CH:11]=1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1参加物
5
実験手順
In acetic acid (15 mL) was stirred 5-nitroisophthalic acid dibenzyl ester (1.3 g, 3.3 mmol). To this was added in parts zinc dust (1.75 g, 26.6 mmol). The mixture was stirred at room temperature for 18 hours. The mixture was filtered free of insoluble material and the acetic acid solution evaporated at reduced pressure. This residue was dissolved in ethyl acetate (120 mL) and washed successively with saturated sodium bicarbonate solution (50 mL), water (50 mL), and brine (50 mL). The organic phase was dried over magnesium sulfate and evaporated in vacuo to give a solid. The solid was stirred into ether (75 mL) and brought to reflux. The solution allowed to recrystallize to give 260 mg (22%) of a white solid. MS: M+1=362.2.
後処理
- filtrationThe mixture was filtered free of insoluble material
- customthe acetic acid solution evaporated at reduced pressure
- dissolutionThis residue was dissolved in ethyl acetate (120 mL)
- washwashed successively with saturated sodium bicarbonate solution (50 mL), water (50 mL), and brine (50 mL)
- dry with materialThe organic phase was dried over magnesium sulfate
- customevaporated in vacuo
- customto give a solid
- temperatureto reflux
- customto recrystallize
出典と根拠
- ORDレコード
- ord-733def17de0f4c6ea64fa843d7cb3d57
- 出典データセット
- uspto-grants-2006_02
- 特許番号
- US06995151B2
反応ノート
読み込み中…