Technology Process of methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate
There total 7 articles about methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
5-methoxy-2-methoxycarbonylmethyl-benzoic acid methyl ester;
With
n-butyllithium; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran;
at -78 - 0 ℃;
for 1.16667h;
Inert atmosphere;
With
carbon dioxide;
In
tetrahydrofuran;
for 1h;
N-benzyloxyamine;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: nitric acid / 2 h / 0 - 22 °C
2.1: methanol; hydrogen / 5%-palladium/activated carbon / 0.08 h / 760.05 Torr / Reflux
3.1: sulfuric acid; sodium nitrite / water / 2 h / 0 - 5 °C / Cooling with ice
4.1: thionyl chloride / 24 h / Reflux
4.2: 12 h / Reflux
5.1: n-butyllithium; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.17 h / -78 - 0 °C / Inert atmosphere
5.2: 1 h
With
methanol; n-butyllithium; thionyl chloride; sulfuric acid; hydrogen; nitric acid; N-ethyl-N,N-diisopropylamine; sodium nitrite;
5%-palladium/activated carbon;
In
tetrahydrofuran; water;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: methanol; hydrogen / 5%-palladium/activated carbon / 0.08 h / 760.05 Torr / Reflux
2.1: sulfuric acid; sodium nitrite / water / 2 h / 0 - 5 °C / Cooling with ice
3.1: thionyl chloride / 24 h / Reflux
3.2: 12 h / Reflux
4.1: n-butyllithium; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.17 h / -78 - 0 °C / Inert atmosphere
4.2: 1 h
With
methanol; n-butyllithium; thionyl chloride; sulfuric acid; hydrogen; N-ethyl-N,N-diisopropylamine; sodium nitrite;
5%-palladium/activated carbon;
In
tetrahydrofuran; water;