反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N+:8]([O-])=O)[C:3]=1[NH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>CCOC(C)=O.[Pd]>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH2:8])[C:3]=1[NH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1参加物
4
実験手順
A mixture of (2-methyl-6-nitrophenyl)phenylamine (981 mg, 4.3 mmol) and 10% Pd/C (981 mg) in EtOAc (20 mL) was degassed with a stream of nitrogen and then stirred at RT under a hydrogen atmosphere for 4 h. The suspension was then filtered through a PTFE frit and the filtrate was concentrated in vacuo affording 3-Methyl-N2-phenylbenzene-1,2-diamine as a yellow solid (852 mg, 100%). LCMS: RT 3.02 min [M+H]+ 199.0
後処理
- customwas degassed with a stream of nitrogen
- filtrationThe suspension was then filtered through a PTFE frit
- concentrationthe filtrate was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-e489c1a362ac4d40849bb7ad10509aba
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08653089B2
関連ノート
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