1: 1.) Mg,I2 / 1 h, reflux 2: 0.675 g / pyridine / 0 °C 3: 1.) sodium iodide, zinc; 2.) dilute acid / 1.) reflux, glyme 4: 1.) HBr; 2.) NaOH / 1.) 15 h, rt., AcOH; 2.) water, reflux, 6 h 5: 1.) acetic acide / 1.) 8 h, reflux 6: 0.01 g / ethyl orthoformate, benzoic acid / 70 - 170 °C View Scheme

1: 1.) Mg,I2 / 1 h, reflux 2: 0.675 g / pyridine / 0 °C 3: 1.) sodium iodide, zinc; 2.) dilute acid / 1.) reflux, glyme 4: 1.) HBr; 2.) NaOH / 1.) 15 h, rt., AcOH; 2.) water, reflux, 6 h View Scheme

With  pyridine; chromium(VI) oxide in  dichloromethane T=20°C; 0.25 h;   

Multi-step reaction with 2 steps 1: perchloric acid2: 1.2 g / CrO3/pyridine / CH2Cl2 / 0.25 h / 20 °C  

Multi-step reaction with 5 steps 1: pyridine2: 3.62 g / lead tetraacetate, iodine / CCl4 3: 1.5 g / Zn/HCl / dioxane4: perchloric acid5: 1.2 g / CrO3/pyridine / CH2Cl2 / 0.25 h / 20 °C  

Multi-step reaction with 6 steps 1: 3.5 g / hydrazine hydrate / ethane-1,2-diol / 140 deg C, 1 h then 195 deg C, 6 h2: pyridine3: 3.62 g / lead tetraacetate, iodine / CCl4 4: 1.5 g / Zn/HCl / dioxane5: perchloric acid6: 1.2 g / CrO3/pyridine / CH2Cl2 / 0.25 h / 20 °C  

Multi-step reaction with 8 steps 1: 1.) triethylamine; 2.) 25percent HCl / 1.) chloroform, 3 h, 35 deg C; 2.) 5 h, reflux2: 85 percent / NaOH / methanol / 1 h / Heating3: 3.5 g / hydrazine hydrate / ethane-1,2-diol / 140 deg C, 1 h then 195 deg C, 6 h4: pyridine5: 3.62 g / lead tetraacetate, iodine / CCl4 6: 1.5 g / Zn/HCl / dioxane7: perchloric acid8: 1.2 g / CrO3/pyridine / CH2Cl2 / 0.25 h / 20 °C  

Multi-step reaction with 3 steps 1: 1.5 g / Zn/HCl / dioxane2: perchloric acid3: 1.2 g / CrO3/pyridine / CH2Cl2 / 0.25 h / 20 °C  

Multi-step reaction with 4 steps 1: 3.62 g / lead tetraacetate, iodine / CCl4 2: 1.5 g / Zn/HCl / dioxane3: perchloric acid4: 1.2 g / CrO3/pyridine / CH2Cl2 / 0.25 h / 20 °C  

Multi-step reaction with 2 steps 1: 1.) Mg,I2 / 1 h, reflux2: 0.675 g / pyridine / 0 °C