Technology Process of (1R,3s,5S)-tert-butyl 3-((1r,4R)-4-hydroxycyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate
There total 3 articles about (1R,3s,5S)-tert-butyl 3-((1r,4R)-4-hydroxycyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
sodium tetraborate decahydrate; palladium 10% on activated carbon; hydrogen;
In
isopropyl alcohol;
at 80 ℃;
for 24h;
under 9000.9 Torr;
Autoclave;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine / tetrahydrofuran / 20 °C / Inert atmosphere; Cooling with ice
2: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 3 h / 20 °C / 1140.08 Torr
3: sodium tetraborate decahydrate; palladium 10% on activated carbon; hydrogen / isopropyl alcohol / 24 h / 80 °C / 9000.9 Torr / Autoclave
With
sodium tetraborate decahydrate; di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; triethylamine; triphenylphosphine;
In
tetrahydrofuran; ethanol; isopropyl alcohol;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine / tetrahydrofuran / 20 °C / Inert atmosphere; Cooling with ice
2: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 3 h / 20 °C / 1140.08 Torr
3: sodium tetraborate decahydrate; palladium 10% on activated carbon; hydrogen / isopropyl alcohol / 24 h / 80 °C / 9000.9 Torr / Autoclave
With
sodium tetraborate decahydrate; di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; triethylamine; triphenylphosphine;
In
tetrahydrofuran; ethanol; isopropyl alcohol;