Technology Process of 4-(tetrahydro-pyran-4-ylmethyl)-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione
There total 5 articles about 4-(tetrahydro-pyran-4-ylmethyl)-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydrogen;
palladium 10% on activated carbon;
In
ethanol;
at 20 ℃;
for 5h;
under 2250.23 Torr;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: potassium phosphate / palladium diacetate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane / toluene / 4 h / 90 °C / Inert atmosphere
2.1: N-ethyl-N,N-diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / 0.83 h / -78 °C / Inert atmosphere
2.2: 1.5 h / -78 - 20 °C
3.1: hydrogenchloride; water / acetone / 1.5 h / 130 °C / microwave irradiation
4.1: hydrogen / palladium 10% on activated carbon / ethanol / 5 h / 20 °C / 2250.23 Torr
With
hydrogenchloride; potassium phosphate; n-butyllithium; water; hydrogen; N-ethyl-N,N-diisopropylamine;
dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium 10% on activated carbon; palladium diacetate;
In
tetrahydrofuran; ethanol; hexane; acetone; toluene;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: potassium phosphate / palladium diacetate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane / toluene / 4 h / 90 °C / Inert atmosphere
2.1: N-ethyl-N,N-diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / 0.83 h / -78 °C / Inert atmosphere
2.2: 1.5 h / -78 - 20 °C
3.1: hydrogenchloride; water / acetone / 1.5 h / 130 °C / microwave irradiation
4.1: hydrogen / palladium 10% on activated carbon / ethanol / 5 h / 20 °C / 2250.23 Torr
With
hydrogenchloride; potassium phosphate; n-butyllithium; water; hydrogen; N-ethyl-N,N-diisopropylamine;
dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium 10% on activated carbon; palladium diacetate;
In
tetrahydrofuran; ethanol; hexane; acetone; toluene;