methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate

Base Information

Chemical Name:methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate
CAS No.:1401606-56-1
Molecular Formula:C₂₇H₄₂O₈Si
Molecular Weight:522.711
Hs Code.:

Synonyms:methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate

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Chemical Property of methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate

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Technology Process of methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate

There total 5 articles about methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate 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%

: 1401606-55-0
methyl 2-(ethoxymethoxy)-4-methoxy-6-(((trifluoromethyl)sulfonyl)oxy)benzoate

: tert-butyl(((4R,5S)-2,2-dimethyl-5-(prop-2-yn-1-yl)-1,3-dioxolan-4-yl)methoxy)dimethylsilane

: 1401606-56-1
methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate

Guidance literature:: With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine; In N,N-dimethyl-formamide; at 20 ℃; for 18h; Inert atmosphere;
DOI:10.1021/ol302498v

Reference yield:

: 19722-76-0
methyl-2,6-dihydroxy-4-methoxybenzoate

: 1401606-56-1
methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

1.2: 18 h / 20 °C

2.1: triethylamine; triphenylphosphine; palladium diacetate; copper(l) iodide / N,N-dimethyl-formamide / 18 h / 20 °C / Inert atmosphere

With copper(l) iodide; palladium diacetate; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol302498v

Reference yield:

: 86795-44-0,86795-47-3,147976-25-8,147976-26-9
3,4-O-isopropylidene-2-deoxy-D-ribose

: 1401606-56-1
methyl 2-(3-((4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-yn-1-yl)-6-(ethoxymethoxy)-4-methoxybenzoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium; diisopropylamine / hexane; tetrahydrofuran / 0.33 h / 0 °C

1.2: 18 h / -78 - 20 °C

2.1: 1H-imidazole / N,N-dimethyl-formamide / 18 h / 20 °C

3.1: triethylamine; triphenylphosphine; palladium diacetate; copper(l) iodide / N,N-dimethyl-formamide / 18 h / 20 °C / Inert atmosphere

With 1H-imidazole; copper(l) iodide; n-butyllithium; palladium diacetate; triethylamine; diisopropylamine; triphenylphosphine; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1021/ol302498v