1,6-二溴-2-甲氧基萘合成路线 (共 14 条)
反应条件
1.1: 89 percent / 2,4,6-collidine; copper(I)iodide / methanol / 19 h / Heating 2.1: 76 percent / Na; EtOH / Heating 3.1: 39.0 g / sodium methoxide / methanol / 2 h / Heating 4.1: LDA / tetrahydrofuran; hexane / 1 h / 0 °C 4.2: 80 percent / tetrahydrofuran; hexane / 1 h / 20 °C 5.1: 43 percent / p-toluenesulfonic acid monohydrate; triethyl orthoformate / CH2Cl2 / 19 h / 25 °C 6.1: 77 percent / potassium bis(trimethylsilyl)amide / diethyl ether; toluene / 2 h / 20 °C 7.1: 80 percent / aq. AcOH / 4 h / Heating 8.1: 97 percent / L-selectride / tetrahydrofuran / 17 h / 0 °C 9.1: diphenylphosphoryl azide; diethyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 17 h / 20 °C 10.1: LiAlH4 / ethanol; diethyl ether / 2 h / 20 °C 11.1: 528 mg / Et3N; DMAP / CH2Cl2 / 17 h / 20 °C 12.1: 83 percent / sodium hydroxide; tetrabutylammonium bromide / toluene; H2O / 0.67 h / 100 °C 13.1: 85 percent / O3; triphenylphosphine / CH2Cl2 / 9 h / -78 - 20 °C 14.1: 92 percent / potassium carbonate; tetrabutylammonium bromide / toluene / 2 h / Heating 15.1: 92 percent / sodium borohydride / ethanol / 1 h / 0 °C 16.1: 70 percent / boron tribromide / CH2Cl2 / 1 h / -40 °C 17.1: Red-Al / toluene / 0.5 h / Heating 18.1: 77 mg / Et3N / CH2Cl2 / 1 h / 25 °C 19.1: 75 percent / hydrogen peroxide / [(C8H17)3NCH3]+3[PO4[W(O)(O2)2]4]3- / 1,2-dichloro-ethane; H2O / 2 h / Heating 20.1: 75 percent / sodium borohydride / ethanol / 2 h / Heating 21.1: sodium periodate; aq. NaHCO3 / tetrahydrofuran / 0.5 h / 25 °C 22.1: 3.9 mg / aq. NaHCO3 / benzene / 0.75 h / Heating 23.1: MnO2 / CH2Cl2 / 0.25 h / 25 °C 23.2: 75 percent / LiAlH4 / tetrahydrofuran / 0.25 h / Heating 24.1: 86 percent / boron tribromide / CHCl3; CH2Cl2 / 0.25 h / 25 °C View Scheme
参考文献
Journal of the American Chemical Society, , vol. 124, # 42 p. 12416 - 12417
反应条件
1.1: 89 percent / 2,4,6-collidine; copper(I)iodide / methanol / 19 h / Heating 2.1: 76 percent / Na; EtOH / Heating 3.1: 39.0 g / sodium methoxide / methanol / 2 h / Heating 4.1: LDA / tetrahydrofuran; hexane / 1 h / 0 °C 4.2: 80 percent / tetrahydrofuran; hexane / 1 h / 20 °C 5.1: 43 percent / p-toluenesulfonic acid monohydrate; triethyl orthoformate / CH2Cl2 / 19 h / 25 °C 6.1: 77 percent / potassium bis(trimethylsilyl)amide / diethyl ether; toluene / 2 h / 20 °C 7.1: 80 percent / aq. AcOH / 4 h / Heating 8.1: 97 percent / L-selectride / tetrahydrofuran / 17 h / 0 °C 9.1: diphenylphosphoryl azide; diethyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 17 h / 20 °C 10.1: LiAlH4 / ethanol; diethyl ether / 2 h / 20 °C 11.1: 528 mg / Et3N; DMAP / CH2Cl2 / 17 h / 20 °C 12.1: 83 percent / sodium hydroxide; tetrabutylammonium bromide / toluene; H2O / 0.67 h / 100 °C 13.1: 85 percent / O3; triphenylphosphine / CH2Cl2 / 9 h / -78 - 20 °C 14.1: 92 percent / potassium carbonate; tetrabutylammonium bromide / toluene / 2 h / Heating 15.1: 92 percent / sodium borohydride / ethanol / 1 h / 0 °C 16.1: 70 percent / boron tribromide / CH2Cl2 / 1 h / -40 °C 17.1: Red-Al / toluene / 0.5 h / Heating 18.1: 77 mg / Et3N / CH2Cl2 / 1 h / 25 °C 19.1: 75 percent / hydrogen peroxide / [(C8H17)3NCH3]+3[PO4[W(O)(O2)2]4]3- / 1,2-dichloro-ethane; H2O / 2 h / Heating 20.1: 75 percent / sodium borohydride / ethanol / 2 h / Heating 21.1: sodium periodate; aq. NaHCO3 / tetrahydrofuran / 0.5 h / 25 °C 22.1: 3.9 mg / aq. NaHCO3 / benzene / 0.75 h / Heating 23.1: MnO2 / CH2Cl2 / 0.25 h / 25 °C 23.2: 75 percent / LiAlH4 / tetrahydrofuran / 0.25 h / Heating View Scheme
参考文献
Taber, Douglass F.; Neubert, Timothy D.; Rheingold, Arnold L.
Journal of the American Chemical Society, 2002 , vol. 124, # 42 p. 12416 - 12417
反应条件
T=100°C; Rate constant;
参考文献
Kolhatkar; Bapat
Journal of the University of Bombay, Science: Physical Sciences, Mathematics, Biological Sciences and Medicine, 1938 , vol. 7/3, p. 157,163, 164, 165
反应条件
N-bromosuccimimide in tetrahydrofuran
2 h; Heating;
参考文献
Hartmann, Rolf; Frotscher, Martin; Oberwinkler, Sandrine; Ziegler, Erika; Messinger, Josef; Thole, Heinrich-Hubert
Patent: US2010/204234 A1, 2010 ;
Location in patent: Page/Page column 15 ;
US 20100204234 A1
反应条件
methanol; potassium hydroxide
T=100°C;
参考文献
Davis
Journal of the Chemical Society, 1900 , vol. 77, p. 37
反应条件
bromine; acetic acid
参考文献
Quelet; Paty
Bulletin de la Societe Chimique de France, 1942 , vol. <5> 9, p. 57
反应条件
bromine; acetic acid
参考文献
Nolan; Smiles
Journal of the Chemical Society, 1913 , vol. 103, p. 345
反应条件
1: tin; hydrochloric acid; alcohol
2: glacial acetic acid; bromine
3: KOH-solution
View Scheme
参考文献
Franzen; Staeuble
Journal fuer Praktische Chemie (Leipzig), 1921 , vol. <2> 103, p. 367
反应条件
1: glacial acetic acid; bromine
2: KOH-solution
View Scheme
参考文献
Franzen; Staeuble
Journal fuer Praktische Chemie (Leipzig), 1921 , vol. <2> 103, p. 367
参考文献
Franzen; Staeuble
Journal fuer Praktische Chemie (Leipzig), 1921 , vol. <2> 103, p. 367