C₃₁H₄₀NO₆P

Base Information

Chemical Name:C₃₁H₄₀NO₆P
CAS No.:1313733-94-6
Molecular Formula:C₃₁H₄₀NO₆P
Molecular Weight:553.635
Hs Code.:

C<sub>31</sub>H<sub>40</sub>NO<sub>6</sub>P

Synonyms:C₃₁H₄₀NO₆P

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Chemical Property of C₃₁H₄₀NO₆P

Chemical Property:

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Technology Process of C₃₁H₄₀NO₆P

There total 4 articles about C₃₁H₄₀NO₆P 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: 71.0%

: 1313733-92-4
C₂₉H₃₈NO₅P

: 75-36-5
acetyl chloride

: 1313733-94-6
C₃₁H₄₀NO₆P

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1021/jm2000085

Reference yield:

: 1-(2-(benzyloxy)ethyl)-2-bromobenzene

: 1313733-94-6
C₃₁H₄₀NO₆P

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium chloride; tetrabutylammonium acetate; palladium diacetate; potassium carbonate / N,N-dimethyl-formamide / 4 h / 90 °C

2.1: phenol / 6 h / 100 °C

2.2: 24 h / Reflux

3.1: pyridine; ethanol / 20 °C

3.2: 0.5 h / 20 °C

3.3: 2 h / 0 - 20 °C

4.1: triethylamine / dichloromethane / 3 h / 20 °C

With potassium chloride; tetrabutylammonium acetate; palladium diacetate; potassium carbonate; triethylamine; phenol; In pyridine; ethanol; dichloromethane; N,N-dimethyl-formamide; 1.1: Mizoroki-Heck reaction;
DOI:10.1021/jm2000085

Reference yield:

: 1313733-76-4
(E)-3-(2-(2-(benzyloxy)ethyl)phenyl)acrylaldehyde

: 1313733-94-6
C₃₁H₄₀NO₆P

Guidance literature:: Multi-step reaction with 3 steps

1.1: phenol / 6 h / 100 °C

1.2: 24 h / Reflux

2.1: pyridine; ethanol / 20 °C

2.2: 0.5 h / 20 °C

2.3: 2 h / 0 - 20 °C

3.1: triethylamine / dichloromethane / 3 h / 20 °C

With triethylamine; phenol; In pyridine; ethanol; dichloromethane;
DOI:10.1021/jm2000085