3-[4-(4,4,5,5-四甲基-[1,3,2]二噁硼烷-2-基)苯基]丙酸甲酯合成路线 (共 8 条)
反应条件
1: 3-(4'-bromophenyl)propionic acid; diazomethyl-trimethyl-silane in methanol; diethyl ether; toluene
T=20°C; 0.25 h;
2: 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-4',4',5',5'-tetramethyl-1,3,2-dioxaborolane With potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride in dimethyl sulfoxide
T=80°C; 2 h;
参考文献
CHUGAI SEIYAKU KABUSHIKI KAISHA
Patent: EP1894911 A1, 2008 ;
Location in patent: Page/Page column 37 ;
反应条件
(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; 1-n-butyl-3-methylimidazolium tetrafluoroborate
T=100°C; 2 h;
参考文献
Zaidlewicz, Marek; Wolan, Andrzej
Journal of Organometallic Chemistry, 2002 , vol. 657, # 1-2 p. 129 - 135
反应条件
[1,3-bis(diphenylphosphino) propane] dichloronickel(II); 1,3-bis-(diphenylphosphino)propane; triethylamine in toluene
T=100°C; 18 h; Inert atmosphere;
参考文献
Rosen, Brad M.; Huang, Chenghong; Percec, Virgil
Organic Letters, 2008 , vol. 10, # 12 p. 2597 - 2600
反应条件
1.1: 78 percent / sodium hydrogensulfate; p-hydroquinone; 4-tert-butylcatechol / diethyl ether / 3 h / 200 °C
2.1: BMS / bis-(2-methoxy-ethyl) ether / 3.5 h / 0 - 140 °C
2.2: aq. NaOH; H2O2 / 3 h / 25 - 50 °C
3.1: CrO3; aq. H2SO4 / acetone / 0.5 h / 20 °C
4.1: 80 percent / thionyl chloride / 2 h / Heating
5.1: 88 percent / PdCl2(dppf); 1-butyl-3-methylimidazolium tetrafluoroborate; potassium acetate / 2 h / 100 °C
View Scheme
参考文献
Zaidlewicz, Marek; Wolan, Andrzej
Journal of Organometallic Chemistry, 2002 , vol. 657, # 1-2 p. 129 - 135
反应条件
1.1: BMS / bis-(2-methoxy-ethyl) ether / 3.5 h / 0 - 140 °C
1.2: aq. NaOH; H2O2 / 3 h / 25 - 50 °C
2.1: CrO3; aq. H2SO4 / acetone / 0.5 h / 20 °C
3.1: 80 percent / thionyl chloride / 2 h / Heating
4.1: 88 percent / PdCl2(dppf); 1-butyl-3-methylimidazolium tetrafluoroborate; potassium acetate / 2 h / 100 °C
View Scheme
参考文献
Zaidlewicz, Marek; Wolan, Andrzej
Journal of Organometallic Chemistry, 2002 , vol. 657, # 1-2 p. 129 - 135
反应条件
1: CrO3; aq. H2SO4 / acetone / 0.5 h / 20 °C
2: 80 percent / thionyl chloride / 2 h / Heating
3: 88 percent / PdCl2(dppf); 1-butyl-3-methylimidazolium tetrafluoroborate; potassium acetate / 2 h / 100 °C
View Scheme
参考文献
Zaidlewicz, Marek; Wolan, Andrzej
Journal of Organometallic Chemistry, 2002 , vol. 657, # 1-2 p. 129 - 135
反应条件
1.1: 76 percent / diethyl ether / 1 h / 20 °C
2.1: 78 percent / sodium hydrogensulfate; p-hydroquinone; 4-tert-butylcatechol / diethyl ether / 3 h / 200 °C
3.1: BMS / bis-(2-methoxy-ethyl) ether / 3.5 h / 0 - 140 °C
3.2: aq. NaOH; H2O2 / 3 h / 25 - 50 °C
4.1: CrO3; aq. H2SO4 / acetone / 0.5 h / 20 °C
5.1: 80 percent / thionyl chloride / 2 h / Heating
6.1: 88 percent / PdCl2(dppf); 1-butyl-3-methylimidazolium tetrafluoroborate; potassium acetate / 2 h / 100 °C
View Scheme
参考文献
Zaidlewicz, Marek; Wolan, Andrzej
Journal of Organometallic Chemistry, 2002 , vol. 657, # 1-2 p. 129 - 135
反应条件
1: 80 percent / thionyl chloride / 2 h / Heating
2: 88 percent / PdCl2(dppf); 1-butyl-3-methylimidazolium tetrafluoroborate; potassium acetate / 2 h / 100 °C
View Scheme
参考文献
Zaidlewicz, Marek; Wolan, Andrzej
Journal of Organometallic Chemistry, 2002 , vol. 657, # 1-2 p. 129 - 135