(R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]oxazolidin-2-one

Base Information

Chemical Name:(R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]oxazolidin-2-one
CAS No.:1120309-12-7
Molecular Formula:C₄₉H₄₉NO₆SSi
Molecular Weight:808.083
Hs Code.:

Synonyms:(R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]oxazolidin-2-one

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Chemical Property of (R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]oxazolidin-2-one

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Technology Process of (R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]oxazolidin-2-one

There total 7 articles about (R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]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:

Reference yield: 92.0%

: 1120309-10-5
(3R)-1-(tert-butyldiphenylsilanyloxy)-6-(trityloxy)hex-4-yn-3-ol

: 4083-64-1
Tosyl isocyanate

: 1120309-12-7
(R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]oxazolidin-2-one

Guidance literature:: With copper(l) iodide; triethylamine; In tetrahydrofuran; at 0 ℃; Reflux;
DOI:10.1016/j.tet.2010.05.050

Reference yield:

: 1120309-51-4
(+/-)-1-(tert-butyldiphenylsilanyloxy)-6-(trityloxy)hex-4-yn-3-ol

: 1120309-12-7
(R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: manganese(IV) oxide / dichloromethane / 15 h / 20 °C

2: (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); isopropyl alcohol / dichloromethane / 1.5 h / 20 °C

3: copper(l) iodide; triethylamine / tetrahydrofuran / 0 °C / Reflux

With manganese(IV) oxide; copper(l) iodide; (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); triethylamine; isopropyl alcohol; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ol8029142

Reference yield:

: 1120309-08-1
1-(tert-butyldiphenylsilanyloxy)-6-(trityloxy)hex-4-yn-3-one

: 1120309-12-7
(R)-5-[2-(tert-butyldiphenylsilanyloxy)ethyl]-3-(toluene-4-sulfonyl)-4-[(Z)-2-trityloxy-ethylidene]oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); isopropyl alcohol / dichloromethane / 1.5 h / 20 °C

2: copper(l) iodide; triethylamine / tetrahydrofuran / 0 °C / Reflux

With copper(l) iodide; (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); triethylamine; isopropyl alcohol; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ol8029142