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C73H122N6O11Si4

Base Information
  • Chemical Name:C73H122N6O11Si4
  • CAS No.:320748-86-5
  • Molecular Formula:C73H122N6O11Si4
  • Molecular Weight:1372.15
  • Hs Code.:
C<sub>73</sub>H<sub>122</sub>N<sub>6</sub>O<sub>11</sub>Si<sub>4</sub>

Synonyms:C73H122N6O11Si4

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Chemical Property of C73H122N6O11Si4
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Technology Process of C73H122N6O11Si4

There total 31 articles about C73H122N6O11Si4 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:
Guidance literature:
Multi-step reaction with 9 steps
1.1: 88 percent / imidazole / tetrahydrofuran / 36 h / 20 °C
2.1: t-BuLi / tetrahydrofuran; pentane / 0.17 h / -78 °C
2.2: 83 percent / CuBr*SMe2; BF3*OEt2 / tetrahydrofuran; pentane / -45 - -20 °C
3.1: imidazole / CH2Cl2 / 11 h / 20 °C
4.1: 289 mg / H2 / Pd/C / ethyl acetate / 50 h / 2280.15 Torr
5.1: 84 percent / Dess-Martin periodinone / CH2Cl2 / 0.75 h / 0 °C
6.1: 93 percent / NaClO2; NaH2PO4*H2O; 2-methyl-2-butene / 2-methyl-propan-2-ol; H2O / 1 h / 0 °C
7.1: diethyl cyanophospinate; iPr2NEt / CH2Cl2 / -30 - -20 °C
7.2: 73 percent / CH2Cl2 / 2 h
8.1: 93 percent / H2 / Pd/C / ethanol / 2 h
9.1: 95 mg / 3-(diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one; iPr2NEt / CH2Cl2
With 1H-imidazole; sodium chlorite; sodium dihydrogenphosphate; diethylphosphoryl cyanide; 2-methyl-but-2-ene; hydrogen; tert.-butyl lithium; Dess-Martin periodane; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water; ethyl acetate; tert-butyl alcohol; pentane; 5.1: Dess-Martin oxidation;
DOI:10.1021/ol006759x
Guidance literature:
Multi-step reaction with 9 steps
1.1: 88 percent / imidazole / tetrahydrofuran / 36 h / 20 °C
2.1: t-BuLi / tetrahydrofuran; pentane / 0.17 h / -78 °C
2.2: 83 percent / CuBr*SMe2; BF3*OEt2 / tetrahydrofuran; pentane / -45 - -20 °C
3.1: imidazole / CH2Cl2 / 11 h / 20 °C
4.1: 289 mg / H2 / Pd/C / ethyl acetate / 50 h / 2280.15 Torr
5.1: 84 percent / Dess-Martin periodinone / CH2Cl2 / 0.75 h / 0 °C
6.1: 93 percent / NaClO2; NaH2PO4*H2O; 2-methyl-2-butene / 2-methyl-propan-2-ol; H2O / 1 h / 0 °C
7.1: diethyl cyanophospinate; iPr2NEt / CH2Cl2 / -30 - -20 °C
7.2: 73 percent / CH2Cl2 / 2 h
8.1: 93 percent / H2 / Pd/C / ethanol / 2 h
9.1: 95 mg / 3-(diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one; iPr2NEt / CH2Cl2
With 1H-imidazole; sodium chlorite; sodium dihydrogenphosphate; diethylphosphoryl cyanide; 2-methyl-but-2-ene; hydrogen; tert.-butyl lithium; Dess-Martin periodane; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water; ethyl acetate; tert-butyl alcohol; pentane; 5.1: Dess-Martin oxidation;
DOI:10.1021/ol006759x
Guidance literature:
Multi-step reaction with 6 steps
1: 81 percent / imidazole / CH2Cl2 / 9 h
2: 86 percent / DMAP; K2CO3 / dimethylformamide / 21 h
3: 88 percent / Bu3SnH; AcOH / Pd(PPh3)4 / CH2Cl2 / 1 h / 0 °C
4: 319 mg / iPr2NEt3; FDPP / CH2Cl2 / 48 h
5: Bu3SnH; AcOH / Pd(PPh3)4 / CH2Cl2 / 0.5 h / 0 °C
6: 95 mg / 3-(diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one; iPr2NEt / CH2Cl2
With 1H-imidazole; dmap; iPr2NEt3; pentafluorophenyl diphenyl-phosphinate; tri-n-butyl-tin hydride; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; tetrakis(triphenylphosphine) palladium(0); In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol006759x
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