Technology Process of methyl (1R,2R)-1-{[(benzyloxy)carbonyl]amino}-2-(2-hydroxyethyl)cyclopropanecarboxylate
There total 10 articles about methyl (1R,2R)-1-{[(benzyloxy)carbonyl]amino}-2-(2-hydroxyethyl)cyclopropanecarboxylate which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
Multi-step reaction with 8 steps
1: hydrogen / palladium on activated charcoal / methanol / 1.5 h / atmospheric pressure
2: trifluoroacetic acid / dichloromethane / Heating
3: TEA / acetone; benzene / 0.5 h / 0 °C
4: sodium azide / acetone / 0.5 h
5: toluene / 2 h / Heating
6: toluene / Heating
7: lithium hydroxide / tetrahydrofuran / 20 °C
8: potassium carbonate / N,N-dimethyl-formamide; acetonitrile
With
lithium hydroxide; sodium azide; TEA; hydrogen; potassium carbonate; trifluoroacetic acid;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; acetonitrile; benzene;
5: Curtius reaction;
DOI:10.1055/s-2005-870007
- Guidance literature:
-
Multi-step reaction with 9 steps
1: sodium hydride / tetrahydrofuran; tert-butyl alcohol / 48 h / 20 °C
2: hydrogen / palladium on activated charcoal / methanol / 1.5 h / atmospheric pressure
3: trifluoroacetic acid / dichloromethane / Heating
4: TEA / acetone; benzene / 0.5 h / 0 °C
5: sodium azide / acetone / 0.5 h
6: toluene / 2 h / Heating
7: toluene / Heating
8: lithium hydroxide / tetrahydrofuran / 20 °C
9: potassium carbonate / N,N-dimethyl-formamide; acetonitrile
With
lithium hydroxide; sodium azide; TEA; hydrogen; sodium hydride; potassium carbonate; trifluoroacetic acid;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; acetonitrile; tert-butyl alcohol; benzene;
6: Curtius reaction;
DOI:10.1055/s-2005-870007
- Guidance literature:
-
Multi-step reaction with 10 steps
1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran
2: sodium hydride / tetrahydrofuran; tert-butyl alcohol / 48 h / 20 °C
3: hydrogen / palladium on activated charcoal / methanol / 1.5 h / atmospheric pressure
4: trifluoroacetic acid / dichloromethane / Heating
5: TEA / acetone; benzene / 0.5 h / 0 °C
6: sodium azide / acetone / 0.5 h
7: toluene / 2 h / Heating
8: toluene / Heating
9: lithium hydroxide / tetrahydrofuran / 20 °C
10: potassium carbonate / N,N-dimethyl-formamide; acetonitrile
With
lithium hydroxide; sodium azide; TEA; hydrogen; sodium hydride; potassium carbonate; triphenylphosphine; trifluoroacetic acid; diethylazodicarboxylate;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; acetonitrile; tert-butyl alcohol; benzene;
1: Mitsunobu reaction / 7: Curtius reaction;
DOI:10.1055/s-2005-870007