Ethylamine → 29526-66-7
反応式
[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][C:3]=1[N+:11]([O-])=O.[CH2:14]([NH2:16])[CH3:15]>C(Cl)Cl>[NH2:11][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:2]=1[CH3:1])[C:6]([NH:16][CH2:14][CH3:15])=[O:7]参加物
4
実験手順
4-methyl-3-nitro-benzoyl chloride (1.0 g, 5.0 mmol) was dissolved in DCM, and the solution was cooled to 0EC. Ethyl amine (2.0M in THF, 5.0 mL, 10 mmol) was added dropwise to the acid chloride, and the reaction stirred at 0EC for 5 min. The ice bath was removed and reaction continued to stir for 3. The solution was washed with brine, dried (Na2SO4), and concentrated in vacuo. The resulting aniline (0.75 g) was used without further purification.
後処理
- temperaturethe solution was cooled to 0EC
- customThe ice bath was removed
- customreaction
- stirringto stir for 3
- washThe solution was washed with brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
- customThe resulting aniline (0.75 g) was used without further purification
出典と根拠
- ORDレコード
- ord-d5e2d6173e7144c698fdce63bee20613
- 出典データセット
- uspto-grants-2009_01
- 特許番号
- US07479495B2
反応ノート
読み込み中…