(R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide

Base Information

Chemical Name:(R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide
CAS No.:1351186-20-3
Molecular Formula:C₂₉H₄₅NO₂Si
Molecular Weight:467.767
Hs Code.:

Synonyms:(R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide

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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 (R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide

Chemical Property:

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Technology Process of (R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide

There total 6 articles about (R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide 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:

: 32231-50-8
(R)-2-methylbutyric acid

: C₂₄H₃₇NOSi

: 1351186-20-3
(R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide

Guidance literature:: With diethyl cyanophosphonate; triethylamine; In dichloromethane; at 20 ℃; for 2.5h; Inert atmosphere;
DOI:10.1021/jo201951s

Reference yield:

: 1351186-26-9
((2R,4S)-6-azido-2,4-dimethylhexyloxy)(tert-butyl)diphenylsilane

: 1351186-20-3
(R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide

Guidance literature:: Multi-step reaction with 2 steps

1: water; triphenylphosphine / tetrahydrofuran / 12 h / 20 - 40 °C

2: diethyl cyanophosphonate; triethylamine / dichloromethane / 2.5 h / 20 °C / Inert atmosphere

With diethyl cyanophosphonate; water; triethylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; 1: Staudinger reaction;
DOI:10.1021/jo201951s

Reference yield:

: 128329-63-5
6-[[(tert-butyl)diphenylsilyl]oxy]-(3S,5R)-3,5-dimethyl-hexan-1-ol

: 1351186-20-3
(R)-N-((3S,5R)-6-(tert-butyldiphenylsilyloxy)-3,5-dimethylhexyl)-2-methylbutanamide

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 3 h / 20 °C / Inert atmosphere

2: sodium azide / N,N-dimethyl-formamide / 12 h / 20 - 40 °C

3: water; triphenylphosphine / tetrahydrofuran / 12 h / 20 - 40 °C

4: diethyl cyanophosphonate; triethylamine / dichloromethane / 2.5 h / 20 °C / Inert atmosphere

With sodium azide; diethyl cyanophosphonate; water; triethylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 3: Staudinger reaction;
DOI:10.1021/jo201951s