Methanol → 2,4-Dichloro-6-methoxymethylbenzylamine
反応式
[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([CH2:11][O:12][CH3:13])[C:3]=1[C:4]#[N:5].CO.[OH-].[Na+]>C1COCC1>[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([CH2:11][O:12][CH3:13])[C:3]=1[CH2:4][NH2:5]参加物
5
反応条件
- 温度
- 60 °C
実験手順
A soln. of BH3 (3.5 mL, 1M in THF) was added to a solution of 2,4-dichloro-6-(methoxymethyl)benzonitrile (0.88 mmol) in 3 mL THF. The reaction mixture was heated to 60° C. for 2 h. At 0° C., 3.5 mL MeOH was dropwise added and the mixture was stirred until gaz evolution was finished. An aq. soln. of 10% NaOH was added still under cooling. The solvent was removed under vacuo, the residue was diluted with water and extracted 3 times with EtOAc. The comb. org. layers were dried over MgSO4 and conc. in vacuo to give the desired product as orange oil.
後処理
- temperatureunder cooling
- customThe solvent was removed under vacuo
- additionthe residue was diluted with water
- extractionextracted 3 times with EtOAc
- dry with materiallayers were dried over MgSO4 and conc. in vacuo
出典と根拠
- ORDレコード
- ord-f6911d267e8d42bd934c956448999d3f
- 出典データセット
- uspto-grants-2016_07
- 特許番号
- US09388197B2
反応ノート
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