1: 3.62 g / lead tetraacetate, iodine / CCl4 2: 1.5 g / Zn/HCl / dioxane 3: perchloric acid 4: 1.2 g / CrO3/pyridine / CH2Cl2 / 0.25 h / 20 °C 5: 1.) Mg,I2 / 1 h, reflux 6: 0.675 g / pyridine / 0 °C 7: 1.) sodium iodide, zinc; 2.) dilute acid / 1.) reflux, glyme 8: 1.) HBr; 2.) NaOH / 1.) 15 h, rt., AcOH; 2.) water, reflux, 6 h 9: 1.) acetic acide / 1.) 8 h, reflux 10: 0.01 g / ethyl orthoformate, benzoic acid / 70 - 170 °C View Scheme

1: 3.62 g / lead tetraacetate, iodine / CCl4 2: 1.5 g / Zn/HCl / dioxane 3: perchloric acid 4: 1.2 g / CrO3/pyridine / CH2Cl2 / 0.25 h / 20 °C 5: 1.) Mg,I2 / 1 h, reflux 6: 0.675 g / pyridine / 0 °C 7: 1.) sodium iodide, zinc; 2.) dilute acid / 1.) reflux, glyme 8: 1.) HBr; 2.) NaOH / 1.) 15 h, rt., AcOH; 2.) water, reflux, 6 h View Scheme

Multi-step reaction with 2 steps 1: 3.5 g / hydrazine hydrate / ethane-1,2-diol / 140 deg C, 1 h then 195 deg C, 6 h2: pyridine  

Multi-step reaction with 4 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: pyridine  

Multi-step reaction with 3 steps 1: 85 percent / NaOH / methanol / 1 h / Heating2: 3.5 g / hydrazine hydrate / ethane-1,2-diol / 140 deg C, 1 h then 195 deg C, 6 h3: pyridine  

With  lead(IV) acetate; iodine in  tetrachloromethane  

Multi-step reaction with 2 steps 1: 3.62 g / lead tetraacetate, iodine / CCl4 2: 1.5 g / Zn/HCl / dioxane  

Multi-step reaction with 3 steps 1: 3.62 g / lead tetraacetate, iodine / CCl4 2: 1.5 g / Zn/HCl / dioxane3: perchloric acid  

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 5 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 °C5: 1.) Mg,I2 / 1 h, reflux