反应 #1973909

反应方程式

Ethyl 2-oxocyclohexanecarboxylate

Bromine

→

3-Bromo-2-hydroxy-1-enecarboxylic

收率 94.4%

3-Bromo-2-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester

收率 94.4%

溶剂

diethyl ether

反应条件

后处理

1. 1
   温度to warm to RT over 90 min
2. 2
   萃取extracted with ethyl acetate (3×200 mL)
3. 3
   干燥The combined organic layers were dried over magnesium sulfate
4. 4
   过滤filtered
5. 5
   浓缩concentrated in vacuo
6. 6
   其他dried on the vacuum line for 18 h

实验过程

Ethyl 2-oxocyclohexanecarboxylate (30 g, 176 mmol, 28 mL) was dissolved in diethyl ether (30 mL) and cooled to 0° C. under nitrogen. Bromine (28 g, 176 mmol, 9.0 mL) was added dropwise over 15 min and the reaction mixture was allowed to warm to RT over 90 min. The mixture was slowly poured into ice-cold saturated aqueous potassium carbonate (250 mL) and extracted with ethyl acetate (3×200 mL). The combined organic layers were dried over magnesium sulfate, filtered, concentrated in vacuo and dried on the vacuum line for 18 h to afford 41.4 g (94%) of 3-Bromo-2-hydroxy-1-enecarboxylic acid ethyl ester (4) as a yellow oil. The structure was confirmed by 13C NMR (75 MHz, CDCl3): δC 14.1, 17.7, 21.8, 32.0, 60.0, 60.8, 99.7, 166.3, and 172.8.

来源