Azobisisobutyronitrile → 2-(Bromomethyl)-4-nitrobenzonitrile
反応式
[CH3:1][C:2]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].[Br:13]N1C(=O)CCC1=O.N(C(C)(C)C#N)=NC(C)(C)C#N>C(Cl)(Cl)(Cl)Cl>[Br:13][CH2:1][C:2]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5]参加物
5
実験手順
A degassed solution of 2-methyl-4-nitrobenzonitrile (10 g, 61.7 mmol), N-bromosuccinimide (13.2 g (74.17 mmol, 1.2 eq.) and azobisisobutyronitrile (AlBN) (2.0 g, 12.18 mmol, 0.2 eq) in 300 ml CCl4 was heated at reflux for 3 days. After solvent was evaporated the residue was taken in ethyl acetate and washed 2× with aq. NaHCO3, aq. Na2S2O3, brine, dried over MgSO4, filtered, concentrated and purified chromatography using 15% ethyl acetate in hexane to provide 11.7 g of 2-bromomethyl-4-nitrobenzonitrile.
後処理
- temperatureat reflux for 3 days
- customAfter solvent was evaporated the residue
- washwashed 2× with aq. NaHCO3, aq. Na2S2O3, brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- custompurified chromatography
出典と根拠
- ORDレコード
- ord-918b183bc3eb4ad1823601baf391f9d4
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08609676B2
反応ノート
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