C₃₀H₄₃O₇P

Base Information

Chemical Name:C₃₀H₄₃O₇P
CAS No.:944913-71-7
Molecular Formula:C₃₀H₄₃O₇P
Molecular Weight:546.641
Hs Code.:

C<sub>30</sub>H<sub>43</sub>O<sub>7</sub>P

Synonyms:C₃₀H₄₃O₇P

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Chemical Property of C₃₀H₄₃O₇P

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Technology Process of C₃₀H₄₃O₇P

There total 7 articles about C₃₀H₄₃O₇P 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: 96.0%

: 944913-70-6
C₂₆H₃₄O₄

: 814-49-3
diethyl chlorophosphate

: 944913-71-7
C₃₀H₄₃O₇P

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 22 ℃; for 4h;
DOI:10.1002/anie.200700501

Reference yield:

: 944913-67-1
C₁₇H₂₂O₃

: 944913-71-7
C₃₀H₄₃O₇P

Guidance literature:: Multi-step reaction with 6 steps

1: NaI / silver(I) complex of chiral N-heterocyclic carbene; (2-iPrO-3-Ph-C₆H₃)CH=RuCl₂(PPh₃) / tetrahydrofuran / 20 h / -15 °C

2: 70 percent / sodium; ammonia; tBuOH / diethyl ether / 0.05 h / -78 °C

3: imidazole / CH₂Cl₂ / 0.75 h / 22 °C

4: (1,3-Mes₂-imidazolidin-2-ylidene)(2-iPrO-benzylidene)RuCl₂ / benzene / 0.67 h / 22 °C

5: 1.034 g / hydrogen peroxide; KF; KHCO₃ / tetrahydrofuran; methanol; H₂O / 22 °C

6: 96 percent / 4-(dimethylamino)pyridine; triethylamine / CH₂Cl₂ / 4 h / 22 °C

With 1H-imidazole; dmap; potassium fluoride; ammonia; dihydrogen peroxide; sodium; potassium hydrogencarbonate; triethylamine; sodium iodide; tert-butyl alcohol; silver(I) complex of chiral N-heterocyclic carbene; (2-iPrO-3-Ph-C₆H₃)CH=RuCl₂(PPh₃); (1,3-Mes₂-imidazolidin-2-ylidene)(2-iPrO-benzylidene)RuCl₂; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; benzene;
DOI:10.1002/anie.200700501

Reference yield:

: 944913-69-3
C₂₅H₃₂O₃

: 944913-71-7
C₃₀H₄₃O₇P

Guidance literature:: Multi-step reaction with 4 steps

1: imidazole / CH₂Cl₂ / 0.75 h / 22 °C

2: (1,3-Mes₂-imidazolidin-2-ylidene)(2-iPrO-benzylidene)RuCl₂ / benzene / 0.67 h / 22 °C

3: 1.034 g / hydrogen peroxide; KF; KHCO₃ / tetrahydrofuran; methanol; H₂O / 22 °C

4: 96 percent / 4-(dimethylamino)pyridine; triethylamine / CH₂Cl₂ / 4 h / 22 °C

With 1H-imidazole; dmap; potassium fluoride; dihydrogen peroxide; potassium hydrogencarbonate; triethylamine; (1,3-Mes₂-imidazolidin-2-ylidene)(2-iPrO-benzylidene)RuCl₂; In tetrahydrofuran; methanol; dichloromethane; water; benzene;
DOI:10.1002/anie.200700501