C₁₇H₁₄N₄O₇

Base Information

Chemical Name:C₁₇H₁₄N₄O₇
CAS No.:1361519-65-4
Molecular Formula:C₁₇H₁₄N₄O₇
Molecular Weight:386.321
Hs Code.:

C<sub>17</sub>H<sub>14</sub>N<sub>4</sub>O<sub>7</sub>

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₁₇H₁₄N₄O₇

Chemical Property:

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Technology Process of C₁₇H₁₄N₄O₇

There total 7 articles about C₁₇H₁₄N₄O₇ 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:

: 1361519-61-0
ethyl 2-(3-hydroxy-4-methoxy-2,6-dinitrophenyl)acetate

: 1361519-65-4
C₁₇H₁₄N₄O₇

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / acetone / 22 h / Reflux

2: water; sodium hydroxide / 1,4-dioxane; ethanol / 0.58 h / 20 °C

3: thionyl chloride / chloroform / 1 h / Reflux

4: tetrahydrofuran; diethyl ether / 1.17 h / 0 - 20 °C / Inert atmosphere

With thionyl chloride; water; potassium carbonate; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; diethyl ether; ethanol; chloroform; acetone;
DOI:10.1002/chem.201102732

Reference yield:

: 1361519-64-3
2-(3-(benzyloxy)-4-methoxy-2,6-dinitrophenyl)acetic acid

: 1361519-65-4
C₁₇H₁₄N₄O₇

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / chloroform / 1 h / Reflux

2: tetrahydrofuran; diethyl ether / 1.17 h / 0 - 20 °C / Inert atmosphere

With thionyl chloride; In tetrahydrofuran; diethyl ether; chloroform;
DOI:10.1002/chem.201102732

Reference yield:

: 90-05-1
2-methoxy-phenol

: 1361519-65-4
C₁₇H₁₄N₄O₇

Guidance literature:: Multi-step reaction with 7 steps

1: nitric acid; acetic acid / diethyl ether; water / 4.42 h / Cooling with ice

2: potassium tert-butylate / N,N-dimethyl-formamide / 1.33 h

3: sulfuric acid / 17 h / 0 °C / Reflux

4: potassium carbonate / acetone / 22 h / Reflux

5: water; sodium hydroxide / 1,4-dioxane; ethanol / 0.58 h / 20 °C

6: thionyl chloride / chloroform / 1 h / Reflux

7: tetrahydrofuran; diethyl ether / 1.17 h / 0 - 20 °C / Inert atmosphere

With thionyl chloride; sulfuric acid; potassium tert-butylate; water; nitric acid; potassium carbonate; acetic acid; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; diethyl ether; ethanol; chloroform; water; N,N-dimethyl-formamide; acetone;
DOI:10.1002/chem.201102732