tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

Base Information

Chemical Name:tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate
CAS No.:1622096-24-5
Molecular Formula:C₃₀H₄₉NO₆Si
Molecular Weight:547.808
Hs Code.:

Synonyms:tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

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Chemical Property of tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

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Technology Process of tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

There total 1 articles about tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate 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: 82.0%

: 1622096-30-3
tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(5-formyl-2-(methoxymethoxy)phenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

: 1779-49-3
Methyltriphenylphosphonium bromide

: 1622096-24-5
tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

Guidance literature:: Methyltriphenylphosphonium bromide; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.25h;

tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(5-formyl-2-(methoxymethoxy)phenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate; In tetrahydrofuran; at 0 ℃; for 0.166667h;
DOI:10.1002/anie.201400286

Reference yield: 93.0%

: 1622096-24-5
tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

: 1622096-25-6
tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-hydroxy-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

Guidance literature:: With zinc dibromide; 1-dodecylthiol; In dichloromethane; at 0 ℃; for 0.166667h;
DOI:10.1002/anie.201400286

Reference yield:

: 1622096-24-5
tert-butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate

: 1622096-26-7
(4aS,4a1R,5S,7aR)-5-((tert-butyldimethylsilyl)oxy)-4a1-(2-(N,4-dimethylphenylsulfonamido)ethyl)-4a,4a1,5,6,7,7a-hexahydro phenanthro[4,5-bcd]furan-3-yl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: zinc dibromide; 1-dodecylthiol / dichloromethane / 0.17 h / 0 °C

2: 1,2-dichloro-ethane / 4 h / Reflux

3: trifluoroacetic acid / dichloromethane / 0.17 h / 0 °C / Cooling with ice

4: triethylamine / dichloromethane / 10 h / 0 - 20 °C

With triethylamine; trifluoroacetic acid; zinc dibromide; 1-dodecylthiol; In dichloromethane; 1,2-dichloro-ethane;
DOI:10.1002/anie.201400286