反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:9])=[C:6](N)[CH:7]=1.N([O-])=O.[Na+].[BrH:14]>O>[Br:14][C:6]1[CH:7]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=1[CH3:9]参加物
反応条件
- 温度
- 0 °C
実験手順
5-chloro-2-methylbenzenamine (50 g, 0.355 mol) was dissolved in HBr solution (1.5 M, 100 mL) and cooled to 0° C., a solution of NaNO2 (27.6 g, 0.4 mol) in water (200 mL) was added dropwise. After addition, the mixture was stirred for 1 hr. In another flask CuBr (30 g, 0.21 mol) was added to HBr solution (1.5 M, 30 mL) and heated to 60° C., then the mixture was added to the above solution. The mixture was heated to reflux for 1 hr then cooled to rt. The reaction was quenched with water (500 mL), the aqueous layer was extracted 3 times with CH2Cl2, dried over Na2SO4, solvent removal and purification by column chromatography afforded 2-bromo-4-chloro-1-methylbenzene (53 g, 0.26 mol). 1H NMR (CDCl3, 400 MHz) δ 7.53 (s, 1H), 7.20-7.10 (m, 2H), 2.36 (s, 3H).
後処理
- additionAfter addition
- temperatureheated to 60° C.
- additionthe mixture was added to the above solution
- temperatureThe mixture was heated
- temperatureto reflux for 1 hr
- temperaturethen cooled to rt
- customThe reaction was quenched with water (500 mL)
- extractionthe aqueous layer was extracted 3 times with CH2Cl2
- dry with materialdried over Na2SO4, solvent removal and purification by column chromatography
出典と根拠
- ORDレコード
- ord-1a6497500bb1438ca1e0c7c71875e548
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08487108B2
関連ノート
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