C₅₉H₁₀₁NO₄

Base Information

Chemical Name:C₅₉H₁₀₁NO₄
CAS No.:1263321-00-1
Molecular Formula:C₅₉H₁₀₁NO₄
Molecular Weight:888.455
Hs Code.:

C<sub>59</sub>H<sub>101</sub>NO<sub>4</sub>

Synonyms:C₅₉H₁₀₁NO₄

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Chemical Property of C₅₉H₁₀₁NO₄

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Technology Process of C₅₉H₁₀₁NO₄

There total 3 articles about C₅₉H₁₀₁NO₄ 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: 60.0%

: 58853-02-4
C₃₀H₅₅NO₂

: 30656-77-0
cholest-5-en-3β-yloxyacetic acid

: 1263321-00-1
C₅₉H₁₀₁NO₄

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In chloroform; for 48h;
DOI:10.1016/j.tet.2010.11.046

Reference yield:

: 58853-01-3
C₃₀H₅₃NO₄

: 1263321-00-1
C₅₉H₁₀₁NO₄

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol; iron; ammonium chloride / 5 h / Reflux

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / chloroform / 48 h

With ethanol; iron; ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In chloroform;
DOI:10.1016/j.tet.2010.11.046

Reference yield:

: 3230-09-9
1,4-bis-dodecyloxy-benzene

: 1263321-00-1
C₅₉H₁₀₁NO₄

Guidance literature:: Multi-step reaction with 3 steps

1: nitric acid; acetic acid / dichloromethane / 2 h / 0 °C

2: ethanol; iron; ammonium chloride / 5 h / Reflux

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / chloroform / 48 h

With ethanol; nitric acid; iron; ammonium chloride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; chloroform;
DOI:10.1016/j.tet.2010.11.046