Multi-step reaction with 8 steps
1.1: diisobutylaluminium hydride / toluene; dichloromethane / 0.5 h / -78 °C
2.1: toluene-4-sulfonic acid / acetone; water / 1 h / 75 °C
3.1: sodium hydride / methanol / 0.5 h / 20 °C
3.2: 20 °C
4.1: sodium hydride / 1,4-dioxane / 0.67 h / 20 - 100 °C / Cooling with ice
5.1: potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 80 °C / Inert atmosphere
6.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium phosphate / water; 1,2-dimethoxyethane; ethanol / Heating
7.1: 10% palladium hydroxide on charcoal; hydrogen / methanol; ethyl acetate / 2 h / 20 °C / 760.05 Torr
8.1: titanium(IV) isopropylate / toluene; ethyl acetate / 48 h / 120 °C / Molecular sieve
With
titanium(IV) isopropylate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; 10% palladium hydroxide on charcoal; hydrogen; potassium acetate; sodium hydride; diisobutylaluminium hydride; toluene-4-sulfonic acid;
In
1,4-dioxane; methanol; 1,2-dimethoxyethane; ethanol; dichloromethane; water; ethyl acetate; acetone; toluene;
3.1: |Wittig Olefination / 3.2: |Wittig Olefination / 5.1: |Suzuki Coupling;