2,2',5,5'-四氯联苯 3,4-氧化物合成路线 (共 10 条)
反应条件
1: 70 percent
2: n-BuLi / 1.) THF, ether, -90 deg C, 0.5 h; 2.) -75 deg C
3: 79 percent / N(Et)3, 2,4-Dinitrobenzenesulfenyl chloride / CH2Cl2 / 0.75 h / Heating
4: m-Chloroperbenzoic acid (85percent) / CCl4 / 0.17 h / 20 - 30 °C
5: NBS, Dibenzoyl peroxide / CCl4 / 7 h / Heating
6: Benzyltriethylammonium chloride / acetonitrile / 22 h / 30 °C
7: 1.) t-BuOCl; 2.) DBU / 1.) CCl4, 4 h, reflux, irradiation; 2.) CH2Cl2, 30 deg C, 2 h
View Scheme
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
1: n-BuLi / 1.) THF, ether, -90 deg C, 0.5 h; 2.) -75 deg C
2: 79 percent / N(Et)3, 2,4-Dinitrobenzenesulfenyl chloride / CH2Cl2 / 0.75 h / Heating
3: m-Chloroperbenzoic acid (85percent) / CCl4 / 0.17 h / 20 - 30 °C
4: NBS, Dibenzoyl peroxide / CCl4 / 7 h / Heating
5: Benzyltriethylammonium chloride / acetonitrile / 22 h / 30 °C
6: 1.) t-BuOCl; 2.) DBU / 1.) CCl4, 4 h, reflux, irradiation; 2.) CH2Cl2, 30 deg C, 2 h
View Scheme
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
1: m-Chloroperbenzoic acid (85percent) / CCl4 / 0.17 h / 20 - 30 °C
2: NBS, Dibenzoyl peroxide / CCl4 / 7 h / Heating
3: Benzyltriethylammonium chloride / acetonitrile / 22 h / 30 °C
4: 1.) t-BuOCl; 2.) DBU / 1.) CCl4, 4 h, reflux, irradiation; 2.) CH2Cl2, 30 deg C, 2 h
View Scheme
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
1: 79 percent / N(Et)3, 2,4-Dinitrobenzenesulfenyl chloride / CH2Cl2 / 0.75 h / Heating
2: m-Chloroperbenzoic acid (85percent) / CCl4 / 0.17 h / 20 - 30 °C
3: NBS, Dibenzoyl peroxide / CCl4 / 7 h / Heating
4: Benzyltriethylammonium chloride / acetonitrile / 22 h / 30 °C
5: 1.) t-BuOCl; 2.) DBU / 1.) CCl4, 4 h, reflux, irradiation; 2.) CH2Cl2, 30 deg C, 2 h
View Scheme
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
1: NBS, Dibenzoyl peroxide / CCl4 / 7 h / Heating
2: Benzyltriethylammonium chloride / acetonitrile / 22 h / 30 °C
3: 1.) t-BuOCl; 2.) DBU / 1.) CCl4, 4 h, reflux, irradiation; 2.) CH2Cl2, 30 deg C, 2 h
View Scheme
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
1: Benzyltriethylammonium chloride / acetonitrile / 22 h / 30 °C
2: 1.) t-BuOCl; 2.) DBU / 1.) CCl4, 4 h, reflux, irradiation; 2.) CH2Cl2, 30 deg C, 2 h
View Scheme
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
tert-butylhypochlorite; 1,8-diazabicyclo[5.4.0]undec-7-ene
1.) CCl4, 4 h, reflux, irradiation; 2.) CH2Cl2, 30 deg C, 2 h; Yield given. Multistep reaction;
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
toluene-4-sulfonic acid in dichloromethane
T=35°C; 0.5 h;
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
toluene-4-sulfonic acid in dichloromethane
T=35°C; 0.5 h;
参考文献
Reich, Ieva L.; Reich, Hans J.
Journal of Organic Chemistry, 1981 , vol. 46, # 18 p. 3721 - 3727
反应条件
toluene-4-sulfonic acid
参考文献
Reich,H.J. et al.
Journal of the American Chemical Society, 1978 , vol. 100, # 18 p. 5981 - 5982