3-(2-溴-4-(全氟甲基)苯基)-3-(4-氟苯基)丙酸合成路线 (共 5 条)
反应条件
1: 82 percent / piperidine / toluene / 0.5 h / Heating
2: 1.) Mg / 1.) ether, 2.) ether, toluene, reflux, 30 min
3: aq. H2SO4, CH3COOH / 24 h / Heating
View Scheme
参考文献
Bogeso
Journal of Medicinal Chemistry, 1983 , vol. 26, # 7 p. 935 - 947
反应条件
sulfuric acid; acetic acid
24 h; Heating; Yield given;
参考文献
Bogeso
Journal of Medicinal Chemistry, 1983 , vol. 26, # 7 p. 935 - 947
反应条件
1: 1.) Mg / 1.) ether, 2.) ether, toluene, reflux, 30 min
2: aq. H2SO4, CH3COOH / 24 h / Heating
View Scheme
参考文献
Bogeso
Journal of Medicinal Chemistry, 1983 , vol. 26, # 7 p. 935 - 947
反应条件
n-butyllithium in diethyl ether; hexane
T=0°C; 0.5 h;
参考文献
Bogeso
Journal of Medicinal Chemistry, 1983 , vol. 26, # 7 p. 935 - 947
反应条件
1: 82 percent / n-butyllithium / hexane; diethyl ether / 0.5 h / 0 °C
2: 75 percent / sodium borohydride / methanol / 1 h / Ambient temperature
3: 100 percent / SOCl2 / toluene / 1.) RT, 30 min, 2.) from 50 deg C to 55 deg C, 1 h
View Scheme
参考文献
Bogeso
Journal of Medicinal Chemistry, 1983 , vol. 26, # 7 p. 935 - 947