N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

Base Information

Chemical Name:N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide
CAS No.:436145-48-1
Molecular Formula:C₂₀H₃₅NO₅Si
Molecular Weight:397.587
Hs Code.:

<i>N</i>-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(<i>tert</i>-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

Synonyms:N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

Suppliers and Price of N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

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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 N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

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Technology Process of N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

There total 1 articles about N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide 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: 87.0%

: 436145-47-0
N-[2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-cyclopent-3-enyl]-acetamide

: 436145-48-1
N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

Guidance literature:: N-[2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-cyclopent-3-enyl]-acetamide; With ozone; In methanol; dichloromethane; at -78 ℃;

With sodium tetrahydroborate; In methanol; dichloromethane; Further stages.;
DOI:10.1021/jo020038p

Reference yield:

: 436145-48-1
N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

: 1053645-62-7
N-[(1S,2R)-2-Benzyloxy-1-((R)-1,2-dihydroxy-ethyl)-3-hydroxy-propyl]-acetamide

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 25 ℃; for 2h;
DOI:10.1021/jo020038p

Reference yield:

: 436145-48-1
N-[1-(1-benzyloxy-2-hydroxy-ethyl)-2-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-propyl]-acetamide

: 436145-50-5
N-[(1S,2R)-2-Benzyloxy-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-oxo-propyl]-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: TBAF / tetrahydrofuran / 2 h / 25 °C

2: 0.043 g / PTSA / acetone / 1 h / 25 °C

3: oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / 3.5 h / -78 - 25 °C

With oxalyl dichloride; tetrabutyl ammonium fluoride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; acetone; 3: Swern oxidation;
DOI:10.1021/jo020038p