反应 #47325

反应方程式

3-trifluoromethyl-phenol

ethyl-2-butynoate

1,8-diazabicyclo[5.4.0]undec-7-ene

→

3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl ester

收率 53.3%

溶剂

tetrahydrofuran

反应条件

后处理

1. 1
   浓缩At this time, the reaction was concentrated in vacuo
2. 2
   workup.DISSOLUTIONThe residue dissolved in dichloromethane (100 mL)
3. 3
   洗涤was washed with a 2N aqueous hydrochloric acid solution (1×100 mL)
4. 4
   干燥The organics were then dried over magnesium sulfate
5. 5
   过滤filtered
6. 6
   洗涤rinsed with dichloromethane
7. 7
   浓缩concentrated in vacuo
8. 8
   其他Purification by Analogix flash chromatography (40 g, 1-10% ethyl acetate/hexanes)

实验过程

A mixture of 3-trifluoromethyl-phenol (1.09 mL, 8.96 mmol) and ethyl-2-butynoate (2.0 g, 17.83 mmol) in tetrahydrofuran (14 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (1.4 mL, 9.37 mmol). The reaction was then heated at 130° C. for 2 h. At this time, the reaction was concentrated in vacuo. The residue dissolved in dichloromethane (100 mL) and was washed with a 2N aqueous hydrochloric acid solution (1×100 mL), a 1N aqueous sodium hydroxide solution (1×100 mL) and a saturated aqueous sodium chloride solution (1×100 mL). The organics were then dried over magnesium sulfate, filtered, rinsed with dichloromethane and concentrated in vacuo. Purification by Analogix flash chromatography (40 g, 1-10% ethyl acetate/hexanes) afforded 3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl ester (1.31 g, 53%) as a clear, colorless oil: HR-ES-MS m/z calculated for C13H13O3F3 [M+H]+ 275.0890, observed 275.0889; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.13 (t, J=7.1 Hz, 3H), 2.45 (s, 3H), 4.01 (q, J=7.1 Hz, 2H), 4.68 (s, 1H), 7.49 (d, J=7.9 Hz, 1H), 7.57 (br. s., 1H), 7.66-7.75 (m, 2H).

来源