反应条件
1: 60 percent / t-butyl hypochlorite / benzene; CHCl3 / 1) 0 deg C, 2 h, 2) r.t., overnight
2: 94 percent / conc. HCl / tetrahydrofuran; H2O / 2 h / Heating
3: 77 percent / ammoniumacetate, / acetic acid; benzene / 30 h / Heating
4: 73 percent / NaOH / H2O / 0.17 h / 65 °C
5: 87 percent / iodine / ethanol / 24 h / Heating
6: 49 percent / Cu powder / quinoline / 1 h / 180 °C
7: 54 percent / pyridine / 3 h / Heating
8: 1) benzoyl peroxide, NBS / 1) CCl4, reflux, 10 h, 2) DMSO
9: 81 percent / K2CO3 / acetone / 18 h / Heating
10: 1) borane/dimethyl sulfide, 2) 1.0 M HCl / 1) THF, 45 min, reflux, 2) CH3OH, reflux
11: 87 percent / sodium acetate / H2O / 0.5 h
View Scheme
参考文献
Campaigne; Smith Jr.; Sandhu; Kim
Journal of Heterocyclic Chemistry, 1983 , vol. 20, # 1 p. 55 - 59