C₅₀H₇₁N₄O₁₀PSi

Base Information

Chemical Name:C₅₀H₇₁N₄O₁₀PSi
CAS No.:1359983-86-0
Molecular Formula:C₅₀H₇₁N₄O₁₀PSi
Molecular Weight:947.194
Hs Code.:

C<sub>50</sub>H<sub>71</sub>N<sub>4</sub>O<sub>10</sub>PSi

Synonyms:

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Chemical Property of C₅₀H₇₁N₄O₁₀PSi

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Technology Process of C₅₀H₇₁N₄O₁₀PSi

There total 4 articles about C₅₀H₇₁N₄O₁₀PSi 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: 73.0%

: 1359983-90-6
C₄₁H₅₄N₂O₉Si

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

: 1359983-86-0
C₅₀H₇₁N₄O₁₀PSi

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 1h;
DOI:10.1021/ja300044e

Reference yield:

: 1359983-84-8
C₁₄H₂₂N₂O₇

: 1359983-86-0
C₅₀H₇₁N₄O₁₀PSi

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / 16 h / 0 - 20 °C

2: pyridine; silver nitrate / tetrahydrofuran / 8 h / Sonication

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h

With pyridine; silver nitrate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja300044e

Reference yield:

: 3282-30-2
pivaloyl chloride

: 1359983-86-0
C₅₀H₇₁N₄O₁₀PSi

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C

1.2: 0.5 h

2.1: trifluoroacetic acid / water / 4 h

3.1: pyridine / 16 h / 0 - 20 °C

4.1: pyridine; silver nitrate / tetrahydrofuran / 8 h / Sonication

5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h

With pyridine; silver nitrate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/ja300044e