反応式
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[NH2:8].[ClH:9].OO.C([O-])([O-])=O.[K+].[K+]>>[Cl:9][C:4]1[C:3]([NH2:8])=[C:2]([CH3:1])[CH:7]=[CH:6][N:5]=1参加物
5
実験手順
A mixture of 4-methylpyridin-3-amine (0.62 g), 12N hydrogen chloride (3.8 mL) and 30% hydrogen peroxide (0.75 mL) was stirred at 0° C. to room temperature for 1 h. The mixture was neutralized with K2CO3, and the mixture was extracted with AcOEt. The organic layer was dried over MgSO4, and concentrated in vacuo to give 2-chloro-4-methylpyridin-3-amine (0.75 g) as an orange solid.
後処理
- extractionthe mixture was extracted with AcOEt
- dry with materialThe organic layer was dried over MgSO4
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-64f6e6e1b99a4f8cb341f6242a1792fb
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09226921B2
関連ノート
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