2-Diazo-3-oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl ester

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Chemical Name:2-Diazo-3-oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl ester
CAS No.:87616-21-5
Molecular Formula:C₁₃H₁₈N₄O₄
Molecular Weight:294.31
Hs Code.:

Synonyms:2-Diazo-3-oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl ester

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Chemical Property of 2-Diazo-3-oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl ester

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Technology Process of 2-Diazo-3-oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl ester

There total 2 articles about 2-Diazo-3-oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl 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:

Reference yield: 83.0%

: 87616-18-0
3-Oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl ester

: 87616-21-5
2-Diazo-3-oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl ester

Guidance literature:: With p-carboxybenzenesulfonyl azide; triethylamine; In acetonitrile; 1.) 0 deg C, 2.) 90 min room temperature;
DOI:10.1021/jo00175a023

Reference yield:

: 80351-01-5
C₈H₁₂N₂O

: 87616-21-5
2-Diazo-3-oxo-4-[1-(3-oxo-[1,2]diazetidin-1-yl)-cyclohexyl]-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1) sodium hydride, 2) n-butyllithium / 1.) THF, 0 deg C, 2.) 3 h, slowly warmed to room temperature

2: 83 percent / p-carboxybenzenesulfonyl azide, triethylamine / acetonitrile / 1.) 0 deg C, 2.) 90 min room temperature

With n-butyllithium; p-carboxybenzenesulfonyl azide; sodium hydride; triethylamine; In acetonitrile;
DOI:10.1021/jo00175a023