Technology Process of Cyclopropaneacetic acid,
a-[[(1,1-dimethylethoxy)carbonyl]amino]-1-[[(4-methoxyphenyl)methoxy]
methyl]-, 2-cyclopropyl-2-oxoethyl ester
There total 8 articles about Cyclopropaneacetic acid,
a-[[(1,1-dimethylethoxy)carbonyl]amino]-1-[[(4-methoxyphenyl)methoxy]
methyl]-, 2-cyclopropyl-2-oxoethyl ester 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:
-
2-(tert-butoxycarbonylamino)-2-(1-((4-methoxybenzyloxy)methyl)cyclopropyl)acetic acid;
With
potassium hydroxide;
In
methanol; dichloromethane;
for 0.0333333h;
2-bromo-1-cyclopropylethan-1-one;
With
potassium iodide;
In
N,N-dimethyl-formamide;
at 20 ℃;
for 4h;
DOI:10.1016/j.ejmech.2016.08.024
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere
1.2: 6.5 h / 0 - 20 °C / Inert atmosphere
2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.17 h / -78 °C
2.2: 0.5 h
3.1: triethylamine / ethanol; water / 60 °C / Sonication
4.1: barium(II) hydroxide / water / Reflux
5.1: triethylamine / water; 1,4-dioxane / 20 °C
6.1: potassium hydroxide / dichloromethane; methanol / 0.03 h
6.2: 4 h / 20 °C
With
oxalyl dichloride; sodium hydride; dimethyl sulfoxide; triethylamine; potassium hydroxide; barium(II) hydroxide;
In
1,4-dioxane; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
2.1: |Swern Oxidation / 3.1: |Bucherer-Bergs Reaction;
DOI:10.1016/j.ejmech.2016.08.024
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 0 °C
2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere
2.2: 6.5 h / 0 - 20 °C / Inert atmosphere
3.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.17 h / -78 °C
3.2: 0.5 h
4.1: triethylamine / ethanol; water / 60 °C / Sonication
5.1: barium(II) hydroxide / water / Reflux
6.1: triethylamine / water; 1,4-dioxane / 20 °C
7.1: potassium hydroxide / dichloromethane; methanol / 0.03 h
7.2: 4 h / 20 °C
With
lithium aluminium tetrahydride; oxalyl dichloride; sodium hydride; dimethyl sulfoxide; triethylamine; potassium hydroxide; barium(II) hydroxide;
In
tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
3.1: |Swern Oxidation / 4.1: |Bucherer-Bergs Reaction;
DOI:10.1016/j.ejmech.2016.08.024