tert-butyl (1S,2R,5E,7R,9R)-1-(4-hydroxybenzyl)-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate

Base Information

• Chemical Name: tert-butyl (1S,2R,5E,7R,9R)-1-(4-hydroxybenzyl)-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate
• CAS No.: 1224714-45-7
• Molecular Formula: C₂₈H₄₇NO₅
• Molecular Weight: 477.685

Synonyms:tert-butyl (1S,2R,5E,7R,9R)-1-(4-hydroxybenzyl)-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate

Chemical Property of tert-butyl (1S,2R,5E,7R,9R)-1-(4-hydroxybenzyl)-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate

Chemical Property:

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Technology Process of tert-butyl (1S,2R,5E,7R,9R)-1-(4-hydroxybenzyl)-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate

There total 1 articles about tert-butyl (1S,2R,5E,7R,9R)-1-(4-hydroxybenzyl)-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(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: 79.0%

tert-butyl (1S,2R,5E,7R,9R)-1-[4-(allyloxy)benzyl]-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate (1224714-44-6) → tert-butyl (1S,2R,5E,7R,9R)-1-(4-hydroxybenzyl)-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate (1224714-45-7)

Guidance literature:

With morpholine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; at 20 ℃; for 12h; Inert atmosphere;

DOI:10.1016/j.tet.2010.02.034

Reference yield: 90.0%

tert-butyl (1S,2R,5E,7R,9R)-1-(4-hydroxybenzyl)-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate (1224714-45-7) → (2S,3R,6E,8R,10R)-1-(4-hydroxyphenyl)-8,10-dimethyl-2-(methylamino)dodec-6-en-3-ol (832150-38-6)

Guidance literature:

With hydrogenchloride; water; In methanol; at 50 ℃; for 1h; Inert atmosphere;

DOI:10.1016/j.tet.2010.02.034

upstream raw materials:

tert-butyl (1S,2R,5E,7R,9R)-1-[4-(allyloxy)benzyl]-2-(methoxymethoxy)-7,9-dimethylundec-5-enyl(methyl)carbamate

Downstream raw materials:

(2S,3R,6E,8R,10R)-1-(4-hydroxyphenyl)-8,10-dimethyl-2-(methylamino)dodec-6-en-3-ol

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