2-Bromoethanol → 2-(2-Iodo-6-methylpyridin-3-yloxy)ethanol
反応式
[I:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[C:4]([CH3:9])[N:3]=1.Br[CH2:11][CH2:12][OH:13]>[OH-].[Na+]>[I:1][C:2]1[C:7]([O:8][CH2:11][CH2:12][OH:13])=[CH:6][CH:5]=[C:4]([CH3:9])[N:3]=1参加物
4
反応条件
- 温度
- 100 °C
実験手順
2-Iodo-6-methyl-pyridin-3-ol (6.49 g, 27.6 mmol) was dissolved in an aqueous solution of sodium hydroxide (1M, 30 mL). 2-bromoethanol (3.91 mL, 55.2 mmol) was added dropwise and then the solution was heated to 100° C. for 3 hours. The resulting mixture was extracted with chloroform (2×200 mL) and the combined organic phases then back extracted with aqueous sodium hydroxide solution (1M, 50 mL). The organic phase was dried over magnesium sulfate and the volatiles removed in vacuo to afford the desired product (5.26 g) which was used without further purification.
後処理
- extractionThe resulting mixture was extracted with chloroform (2×200 mL)
- extractionthe combined organic phases then back extracted with aqueous sodium hydroxide solution (1M, 50 mL)
- dry with materialThe organic phase was dried over magnesium sulfate
- customthe volatiles removed in vacuo
出典と根拠
- ORDレコード
- ord-dbf02a3f8f8448e18c63e2fd8cf688b5
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07141564B2
反応ノート
読み込み中…