(1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol

Base Information

Chemical Name:(1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol
CAS No.:223384-27-8
Molecular Formula:C₃₁H₄₃NO₂Si
Molecular Weight:489.773
Hs Code.:

Synonyms:(1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol

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Technology Process of (1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol

There total 1 articles about (1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol 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: 89.0%

: 138611-10-6
(2R,3R)-3-Hexylamino-3-phenyl-propane-1,2-diol

: 58479-61-1
tert-butylchlorodiphenylsilane

: 223384-27-8
(1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol

Guidance literature:: With 1H-imidazole; In tetrahydrofuran; for 5h; Ambient temperature;
DOI:10.1016/S0040-4039(99)00219-1

Reference yield: 92.0%

: 32315-10-9
bis(trichloromethyl) carbonate

: 223384-27-8
(1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol

: 223384-28-9
(4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-3-hexyl-4-phenyl-oxazolidin-2-one

Guidance literature:: With triethylamine; In dichloromethane; for 12h; Ambient temperature;
DOI:10.1016/S0040-4039(99)00219-1

Reference yield:

: 223384-27-8
(1R,2R)-3-(t-butyldiphenylsiloxy)-1-phenyl-1-N-(n-hexylamino)-2-propanol

: (S)-N-(1-phenyl-2-propenyl)-n-hexylamine

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / Et₃N / CH₂Cl₂ / 12 h / Ambient temperature

2: 70 percent / Bu₄NF / tetrahydrofuran / 3 h / Ambient temperature

3: 93 percent / Et₃N, DMAP / CH₂Cl₂ / 3 h / Ambient temperature

4: 95 percent / Te, NaBH₄, Adogen 464 / toluene; H₂O / 24 h / Ambient temperature

With dmap; tellurium; sodium tetrahydroborate; adogen 464; tetrabutyl ammonium fluoride; triethylamine; In tetrahydrofuran; dichloromethane; water; toluene;
DOI:10.1016/S0040-4039(99)00219-1