Technology Process of (R)-3-(3-(benzyloxy)propyl)morpholine
There total 3 articles about (R)-3-(3-(benzyloxy)propyl)morpholine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
2-((5-(benzyloxy)pent-2-yn-1-yl)oxy)ethanamine;
With
C42H58N4O2Ti;
In
toluene;
at 110 ℃;
for 14h;
Inert atmosphere;
Schlenk technique;
With
formic acid; [{(1S,2S-N-p-toluenesulfonyl-1,2-diphenylethanediamine)}(η6-p-cymene)RuCl]; triethylamine;
In
N,N-dimethyl-formamide; toluene;
at 20 ℃;
for 14h;
enantioselective reaction;
Inert atmosphere;
Schlenk technique;
DOI:10.1002/anie.201206826
- Guidance literature:
-
With
[(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); formic acid; triethylamine;
In
N,N-dimethyl-formamide;
at 23 ℃;
enantioselective reaction;
Inert atmosphere;
Schlenk technique;
DOI:10.1021/acs.joc.6b01884
- Guidance literature:
-
Multi-step reaction with 4 steps
1: tetra-(n-butyl)ammonium iodide; sodium iodide; potassium hydroxide / tetrahydrofuran / 24 h / Reflux
2: methanol / 0 - 23 °C
3: bis(N-2,6-diisoprpylphenylbenzamidato)bis(dimethylamido)titanium (IV) / toluene / 14 h / 110 °C / Inert atmosphere; Glovebox; Schlenk technique; Sealed tube
4: formic acid; [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); triethylamine / N,N-dimethyl-formamide / 23 °C / Inert atmosphere; Schlenk technique
With
[(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); formic acid; bis(N-2,6-diisoprpylphenylbenzamidato)bis(dimethylamido)titanium (IV); tetra-(n-butyl)ammonium iodide; triethylamine; sodium iodide; potassium hydroxide;
In
tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene;
1: |Williamson Ether Synthesis;
DOI:10.1021/acs.joc.6b01884