estere metilico dell'acido cis-N-benzoil-4-<4-(1-etossicarboniletil)fenilammino>cicloesancarbonico

Base Information

Chemical Name:estere metilico dell'acido cis-N-benzoil-4-<4-(1-etossicarboniletil)fenilammino>cicloesancarbonico
CAS No.:94593-55-2
Molecular Formula:C₂₆H₃₁NO₅
Molecular Weight:437.536
Hs Code.:

Synonyms:

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Chemical Property of estere metilico dell'acido cis-N-benzoil-4-<4-(1-etossicarboniletil)fenilammino>cicloesancarbonico

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Technology Process of estere metilico dell'acido cis-N-benzoil-4-<4-(1-etossicarboniletil)fenilammino>cicloesancarbonico

There total 4 articles about estere metilico dell'acido cis-N-benzoil-4-<4-(1-etossicarboniletil)fenilammino>cicloesancarbonico 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:

: 6297-22-9
4-carbomethoxycyclohexanone

: 94593-55-2
estere metilico dell'acido cis-N-benzoil-4-<4-(1-etossicarboniletil)fenilammino>cicloesancarbonico

Guidance literature:: Multi-step reaction with 2 steps

1: benzene / 24 h / Heating

2: triethylamine / dioxane / 24 h / Ambient temperature

With triethylamine; In 1,4-dioxane; benzene;

Reference yield:

: 32868-25-0
2-(4-amminofenil)propionico d'etile

: 94593-55-2
estere metilico dell'acido cis-N-benzoil-4-<4-(1-etossicarboniletil)fenilammino>cicloesancarbonico

Guidance literature:: Multi-step reaction with 2 steps

1: benzene / 24 h / Heating

2: triethylamine / dioxane / 24 h / Ambient temperature

With triethylamine; In 1,4-dioxane; benzene;

Reference yield:

: 3618-03-9,6125-57-1,17449-76-2
methyl 4-hydroxycyclohexanecarboxylate

: 94593-55-2
estere metilico dell'acido cis-N-benzoil-4-<4-(1-etossicarboniletil)fenilammino>cicloesancarbonico

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / chromic anhydride, 30percent H₂SO₄ / acetone; H₂O / 5 h / Ambient temperature

2: benzene / 24 h / Heating

3: triethylamine / dioxane / 24 h / Ambient temperature

With chromium(VI) oxide; sulfuric acid; triethylamine; In 1,4-dioxane; water; acetone; benzene;