Multi-step reaction with 7 steps
1.1: potassium hydroxide / ethanol; water / 2.08 h / 100 °C
1.2: Cooling with ice
1.3: pH 1
2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 0 °C
2.2: 0 - 20 °C
3.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 100 °C / Reflux
4.1: acetonitrile
5.1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane; water / 0.17 h / 160 °C / Microwave irradiation
6.1: potassium hydroxide; water / methanol / 90 °C
6.2: pH 6 / Cooling with ice
7.1: N-ethyl-N,N-diisopropylamine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / dichloromethane; ethyl acetate
With
N-Bromosuccinimide; oxalyl dichloride; water; sodium carbonate; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; potassium hydroxide; dibenzoyl peroxide;
dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; N,N-dimethyl-formamide;
In
1,4-dioxane; methanol; tetrachloromethane; ethanol; dichloromethane; water; ethyl acetate; acetonitrile;
5.1: Suzuki Coupling;