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(2R*,3S*)-2,3-bis<4-<(tert-butyldimethylsilyl)oxy>phenyl>pentyl 4-aminobutyl sulfide

Base Information
  • Chemical Name:(2R*,3S*)-2,3-bis<4-<(tert-butyldimethylsilyl)oxy>phenyl>pentyl 4-aminobutyl sulfide
  • CAS No.:104947-05-9
  • Molecular Formula:C33H57NO2SSi2
  • Molecular Weight:588.058
  • Hs Code.:
(2R*,3S*)-2,3-bis<4-<(tert-butyldimethylsilyl)oxy>phenyl>pentyl 4-aminobutyl sulfide

Synonyms:(2R*,3S*)-2,3-bis<4-<(tert-butyldimethylsilyl)oxy>phenyl>pentyl 4-aminobutyl sulfide

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Chemical Property of (2R*,3S*)-2,3-bis<4-<(tert-butyldimethylsilyl)oxy>phenyl>pentyl 4-aminobutyl sulfide
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Technology Process of (2R*,3S*)-2,3-bis<4-<(tert-butyldimethylsilyl)oxy>phenyl>pentyl 4-aminobutyl sulfide

There total 8 articles about (2R*,3S*)-2,3-bis<4-<(tert-butyldimethylsilyl)oxy>phenyl>pentyl 4-aminobutyl sulfide 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 8 steps
1: 99 percent / NaH, EtSH / dimethylformamide / 19 h / 120 °C
2: 89 percent / imidazole / dimethylformamide / 1 h
3: diethyl ether; hexane / 20 h / Ambient temperature
4: 1.) BH3*THF, 2.) H2O, NaOH, H2O2 / 1.) THF, 0 deg C, 4.5 h, 2.) THF, from 45 to 50 deg C, 1 h
5: 76 percent / Ph3P, diisopropyl azodicarboxylate / tetrahydrofuran / 5 h / 0 °C
6: 58 percent / LiAlH4 / diethyl ether / 0.08 h / 0 °C
7: 90 percent / KH / tetrahydrofuran / 1.25 h / -78 - 20 °C
8: 68 percent / LiAlH4 / tetrahydrofuran / 24 h / Ambient temperature
With 1H-imidazole; sodium hydroxide; lithium aluminium tetrahydride; borane-THF; di-isopropyl azodicarboxylate; water; dihydrogen peroxide; potassium hydride; sodium hydride; triphenylphosphine; ethanethiol; In tetrahydrofuran; diethyl ether; hexane; N,N-dimethyl-formamide;
DOI:10.1021/jm00384a026
Guidance literature:
Multi-step reaction with 7 steps
1: 89 percent / imidazole / dimethylformamide / 1 h
2: diethyl ether; hexane / 20 h / Ambient temperature
3: 1.) BH3*THF, 2.) H2O, NaOH, H2O2 / 1.) THF, 0 deg C, 4.5 h, 2.) THF, from 45 to 50 deg C, 1 h
4: 76 percent / Ph3P, diisopropyl azodicarboxylate / tetrahydrofuran / 5 h / 0 °C
5: 58 percent / LiAlH4 / diethyl ether / 0.08 h / 0 °C
6: 90 percent / KH / tetrahydrofuran / 1.25 h / -78 - 20 °C
7: 68 percent / LiAlH4 / tetrahydrofuran / 24 h / Ambient temperature
With 1H-imidazole; sodium hydroxide; lithium aluminium tetrahydride; borane-THF; di-isopropyl azodicarboxylate; water; dihydrogen peroxide; potassium hydride; triphenylphosphine; In tetrahydrofuran; diethyl ether; hexane; N,N-dimethyl-formamide;
DOI:10.1021/jm00384a026
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