C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅

Base Information

Chemical Name:C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅
CAS No.:200354-19-4
Molecular Formula:C₆₁H₈₁N₅O₄
Molecular Weight:948.345
Hs Code.:

C<sub>12</sub>H<sub>25</sub>OC<sub>6</sub>H<sub>4</sub>OCH<sub>2</sub>C<sub>7</sub>N<sub>2</sub>H<sub>3</sub>(C<sub>2</sub>H<sub>5</sub>)C<sub>5</sub>NH<sub>3</sub>C<sub>7</sub>N<sub>2</sub>H<sub>3</sub>(C<sub>2</sub>H<sub>5</sub>)CH<sub>2</sub>OC<sub>6</sub>H<sub>4</sub>OC<sub>12</sub>H<sub>25</sub>

Synonyms:C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅

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Chemical Property of C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅

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Technology Process of C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅

There total 12 articles about C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅ 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:

: 3739-94-4
2,6-Pyridinedicarbonyl dichloride

: 200354-19-4
C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅

Guidance literature:: Multi-step reaction with 4 steps

1: Et₃N / CH₂Cl₂ / 8 h / Heating

2: 80 percent / Fe, aq. HCl / ethanol / 12 h / Heating

3: 92 percent / BBr₃ / CH₂Cl₂ / 3 h / Ambient temperature

4: 1.) NBu₄OH / 1.) CH₂Cl₂, MeOH, i-PrOH, 2.) CH₂Cl₂, 48 h

With hydrogenchloride; tetra(n-butyl)ammonium hydroxide; boron tribromide; iron; triethylamine; In ethanol; dichloromethane;
DOI:10.1021/ja982545n

Reference yield:

: 218143-44-3
N-ethyl-(4-methoxymethyl-2-nitrophenyl)amine

: 200354-19-4
C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅

Guidance literature:: Multi-step reaction with 4 steps

1: Et₃N / CH₂Cl₂ / 8 h / Heating

2: 80 percent / Fe, aq. HCl / ethanol / 12 h / Heating

3: 92 percent / BBr₃ / CH₂Cl₂ / 3 h / Ambient temperature

4: 1.) NBu₄OH / 1.) CH₂Cl₂, MeOH, i-PrOH, 2.) CH₂Cl₂, 48 h

With hydrogenchloride; tetra(n-butyl)ammonium hydroxide; boron tribromide; iron; triethylamine; In ethanol; dichloromethane;
DOI:10.1021/ja982545n

Reference yield:

: 218143-46-5
bispyridine-2,6-dicarboxamide

: 200354-19-4
C₁₂H₂₅OC₆H₄OCH₂C₇N₂H₃(C₂H₅)C₅NH₃C₇N₂H₃(C₂H₅)CH₂OC₆H₄OC₁₂H₂₅

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / Fe, aq. HCl / ethanol / 12 h / Heating

2: 92 percent / BBr₃ / CH₂Cl₂ / 3 h / Ambient temperature

3: 1.) NBu₄OH / 1.) CH₂Cl₂, MeOH, i-PrOH, 2.) CH₂Cl₂, 48 h

With hydrogenchloride; tetra(n-butyl)ammonium hydroxide; boron tribromide; iron; In ethanol; dichloromethane;
DOI:10.1021/ja982545n