Multi-step reaction with 8 steps
1.1: n-butyllithium; 2,2,6,6-tetramethylpiperidinyl-lithium / tetrahydrofuran; hexane / 0.08 h / -78 - -10 °C / Inert atmosphere
1.2: 5 h / -78 - 20 °C / Inert atmosphere
2.1: toluene / 20 °C
3.1: tetrakis(triphenylphosphine) palladium(0); potassium carbonate / ethanol; toluene / 4 h / 100 °C / Inert atmosphere
4.1: hydrogenchloride; water / 12 h / Reflux
5.1: oxalyl dichloride / dichloromethane / 3 h / 0 - 20 °C
5.2: 1 h / 10 - 20 °C
6.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 8 h / Reflux
7.1: acetonitrile / 3 h / Reflux; Inert atmosphere
8.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 85 °C / Sealed tube
With
hydrogenchloride; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium(0); n-butyllithium; oxalyl dichloride; 2,2,6,6-tetramethylpiperidinyl-lithium; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; dibenzoyl peroxide;
In
tetrahydrofuran; tetrachloromethane; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;
3.1: |Suzuki Coupling;
DOI:10.1016/j.ejmech.2012.07.040