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C52H82O8Si2

Base Information
  • Chemical Name:C52H82O8Si2
  • CAS No.:220691-98-5
  • Molecular Formula:C52H82O8Si2
  • Molecular Weight:891.389
  • Hs Code.:
C<sub>52</sub>H<sub>82</sub>O<sub>8</sub>Si<sub>2</sub>

Synonyms:C52H82O8Si2

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Chemical Property of C52H82O8Si2
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Technology Process of C52H82O8Si2

There total 37 articles about C52H82O8Si2 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:
With ammonium cerium(IV) nitrate; water; In tetrahydrofuran; acetonitrile; at 0 ℃;
Guidance literature:
Multi-step reaction with 16 steps
1: 84 percent / Ph3P, DEAD / tetrahydrofuran / Heating
2: 98 percent / DIBAL-H / toluene / -78 °C
3: acetonitrile
4: NaOH / H2O / Heating
5: 1.) LDA, 2.) t-BuOK / 1.) THF, -78 deg C, 2.) THF, -78 deg C to r.t.
6: H2O, TFA / CH2Cl2
7: 87 percent / imidazole / dimethylformamide
8: 96 percent / MCPBA, NaOAc / CH2Cl2 / 0 °C
9: 1.) BuLi, Me2AlCl / 1.) PhMe, 0 deg C; CH2Cl2, 0 deg C to r.t., 2.) PhMe, CH2Cl2
10: 1.) 9-BBN, 2.) NaOH, H2O2 / 1.) THF, reflux, 2.) THF, H2O2, r.t.
11: NaBH4 / ethanol / 0 °C
12: 95 percent / 2,6-lutidine / CH2Cl2
13: 95 percent / H2 / Pd/C / methanol; CH2Cl2
14: 97 percent / TPAP, NMO, molecular sieves 4 Angstroem / CH2Cl2
15: 90 percent / toluene / Heating
16: 98 percent / CAN, H2O / acetonitrile; tetrahydrofuran / 0 °C
With 1H-imidazole; 2,6-dimethylpyridine; sodium hydroxide; sodium tetrahydroborate; 9-borabicyclo[3.3.1]nonane dimer; n-butyllithium; N-methyl-2-indolinone; tetrapropylammonium perruthennate; ammonium cerium(IV) nitrate; 4 A molecular sieve; potassium tert-butylate; water; hydrogen; dihydrogen peroxide; sodium acetate; dimethylaluminum chloride; diisobutylaluminium hydride; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; trifluoroacetic acid; lithium diisopropyl amide; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 19 steps
1: 1.) 9-BBN, 2.) NaOH, H2O2 / 1.) THF, 65 deg C, 2.) THF, H2O, 0 deg C to r.t.
2: 96 percent / PPTS / CH2Cl2
3: Na, NH3 / diethyl ether
4: PPTS / CH2Cl2
5: Et3N / CH2Cl2 / -5 °C
6: NaI, molecular sieves 4 Angstroem / butan-2-one / 45 °C
7: 1.) BuLi, DMPU / 1.) THF, -78 deg C, 2.) THF
8: CSA / methanol
9: TPAP, NMO, molecular sieves 4 Angstroem / CH2Cl2
10: Ph3P / 0 °C
11: BuLi
12: 1.) BuLi, Me2AlCl / 1.) PhMe, 0 deg C; CH2Cl2, 0 deg C to r.t., 2.) PhMe, CH2Cl2
13: 1.) 9-BBN, 2.) NaOH, H2O2 / 1.) THF, reflux, 2.) THF, H2O2, r.t.
14: NaBH4 / ethanol / 0 °C
15: 95 percent / 2,6-lutidine / CH2Cl2
16: 95 percent / H2 / Pd/C / methanol; CH2Cl2
17: 97 percent / TPAP, NMO, molecular sieves 4 Angstroem / CH2Cl2
18: 90 percent / toluene / Heating
19: 98 percent / CAN, H2O / acetonitrile; tetrahydrofuran / 0 °C
With 2,6-dimethylpyridine; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; sodium hydroxide; sodium tetrahydroborate; 9-borabicyclo[3.3.1]nonane dimer; n-butyllithium; N-methyl-2-indolinone; tetrapropylammonium perruthennate; ammonium cerium(IV) nitrate; 4 A molecular sieve; camphor-10-sulfonic acid; ammonia; water; hydrogen; dihydrogen peroxide; sodium; dimethylaluminum chloride; pyridinium p-toluenesulfonate; triethylamine; triphenylphosphine; sodium iodide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; toluene; acetonitrile; butanone;
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