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(S)-4-Benzyl-3-[(2S,4S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-hexanoyl]-oxazolidin-2-one

Base Information
  • Chemical Name:(S)-4-Benzyl-3-[(2S,4S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-hexanoyl]-oxazolidin-2-one
  • CAS No.:428874-28-6
  • Molecular Formula:C34H43NO4Si
  • Molecular Weight:557.805
  • Hs Code.:
(S)-4-Benzyl-3-[(2S,4S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-hexanoyl]-oxazolidin-2-one

Synonyms:(S)-4-Benzyl-3-[(2S,4S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-hexanoyl]-oxazolidin-2-one

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Chemical Property of (S)-4-Benzyl-3-[(2S,4S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-hexanoyl]-oxazolidin-2-one
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Technology Process of (S)-4-Benzyl-3-[(2S,4S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-hexanoyl]-oxazolidin-2-one

There total 8 articles about (S)-4-Benzyl-3-[(2S,4S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-hexanoyl]-oxazolidin-2-one 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:
(S)-4-Benzyl-3-[(S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-hexanoyl]-oxazolidin-2-one; With sodium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃; for 1h;
methyl iodide; In tetrahydrofuran; at -78 - -40 ℃; Further stages.;
DOI:10.1021/ja020091v
Guidance literature:
Multi-step reaction with 8 steps
1.1: lithium borohydride / diethyl ether; H2O / 0.5 h / 0 °C
2.1: 20.6 g / imidazole; 4 Angstroem molecular sieves / petroleum ether; diethyl ether; dimethylformamide / 20 °C
3.1: 9-BBN / tetrahydrofuran / 4 h / 20 °C
3.2: 92 percent / sodium hydroxide; hydroden peroxide / tetrahydrofuran; H2O / 0 - 20 °C
4.1: pyridinium dichromate / CH2Cl2 / 0.5 h
5.1: 6.9 g / sodium chlorite; sulfamic acid / tetrahydrofuran; H2O / 0 - 20 °C
6.1: triethylamine / tetrahydrofuran / -78 - 0 °C
7.1: 5.53 g / lithium chloride / tetrahydrofuran / 20 °C
8.1: sodium hexamethyldisilazide / tetrahydrofuran / 1 h / -78 °C
8.2: 95 percent / tetrahydrofuran / -78 - -40 °C
With 1H-imidazole; sodium chlorite; dipyridinium dichromate; lithium borohydride; 9-borabicyclo[3.3.1]nonane dimer; 4 A molecular sieve; aminosulfonic acid; sodium hexamethyldisilazane; triethylamine; lithium chloride; In tetrahydrofuran; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide; Petroleum ether;
DOI:10.1021/ja020091v
Guidance literature:
Multi-step reaction with 5 steps
1.1: pyridinium dichromate / CH2Cl2 / 0.5 h
2.1: 6.9 g / sodium chlorite; sulfamic acid / tetrahydrofuran; H2O / 0 - 20 °C
3.1: triethylamine / tetrahydrofuran / -78 - 0 °C
4.1: 5.53 g / lithium chloride / tetrahydrofuran / 20 °C
5.1: sodium hexamethyldisilazide / tetrahydrofuran / 1 h / -78 °C
5.2: 95 percent / tetrahydrofuran / -78 - -40 °C
With sodium chlorite; dipyridinium dichromate; aminosulfonic acid; sodium hexamethyldisilazane; triethylamine; lithium chloride; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/ja020091v
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