C₄₂H₅₁N₄O₁₀P

Base Information

Chemical Name:C₄₂H₅₁N₄O₁₀P
CAS No.:1446748-48-6
Molecular Formula:C₄₂H₅₁N₄O₁₀P
Molecular Weight:802.861
Hs Code.:

C<sub>42</sub>H<sub>51</sub>N<sub>4</sub>O<sub>10</sub>P

Synonyms:C₄₂H₅₁N₄O₁₀P

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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 C₄₂H₅₁N₄O₁₀P

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Technology Process of C₄₂H₅₁N₄O₁₀P

There total 11 articles about C₄₂H₅₁N₄O₁₀P 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: 84.0%

: 1446748-47-5
C₃₃H₃₄N₂O₉

: 124482-92-4,89992-70-1
2-cyanoethyl-N,N-(diisopropylamino)chlorophosphine

: 1446748-48-6
C₄₂H₅₁N₄O₁₀P

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ol401566r

Reference yield:

: 1446748-41-9
C₃₃H₄₆N₂O₉Si

: 1446748-48-6
C₄₂H₅₁N₄O₁₀P

Guidance literature:: Multi-step reaction with 7 steps

1: 2,6-dimethylpyridine / dichloromethane / 1 h / 0 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

3: pyridine / 1 h / 0 °C / Inert atmosphere

4: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 - 20 °C / Inert atmosphere

5: 20% palladium hydroxide-activated charcoal; cyclohexene / ethanol / Reflux; Inert atmosphere

6: pyridine / 0 - 20 °C / Inert atmosphere

7: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

With pyridine; 2,6-dimethylpyridine; 20% palladium hydroxide-activated charcoal; tetrabutyl ammonium fluoride; sodium hydride; N-ethyl-N,N-diisopropylamine; cyclohexene; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1021/ol401566r

Reference yield:

: 1446748-43-1
C₄₈H₅₀N₂O₁₁

: 1446748-48-6
C₄₂H₅₁N₄O₁₀P

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine / 1 h / 0 °C / Inert atmosphere

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 - 20 °C / Inert atmosphere

3: 20% palladium hydroxide-activated charcoal; cyclohexene / ethanol / Reflux; Inert atmosphere

4: pyridine / 0 - 20 °C / Inert atmosphere

5: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

With pyridine; 20% palladium hydroxide-activated charcoal; sodium hydride; N-ethyl-N,N-diisopropylamine; cyclohexene; In ethanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1021/ol401566r