(5S,6R)-5-[(S)-1-methoxy-2-(4-methoxybenzyloxy)ethyl]-2,2,3,3,6,9,9,10,10-nonamethyl-4,8-dioxa-3,9-disilaundecane

Base Information

Chemical Name:(5S,6R)-5-[(S)-1-methoxy-2-(4-methoxybenzyloxy)ethyl]-2,2,3,3,6,9,9,10,10-nonamethyl-4,8-dioxa-3,9-disilaundecane
CAS No.:1262137-87-0
Molecular Formula:C₂₇H₅₂O₅Si₂
Molecular Weight:512.878
Hs Code.:

Synonyms:(5S,6R)-5-[(S)-1-methoxy-2-(4-methoxybenzyloxy)ethyl]-2,2,3,3,6,9,9,10,10-nonamethyl-4,8-dioxa-3,9-disilaundecane

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Chemical Property of (5S,6R)-5-[(S)-1-methoxy-2-(4-methoxybenzyloxy)ethyl]-2,2,3,3,6,9,9,10,10-nonamethyl-4,8-dioxa-3,9-disilaundecane

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Technology Process of (5S,6R)-5-[(S)-1-methoxy-2-(4-methoxybenzyloxy)ethyl]-2,2,3,3,6,9,9,10,10-nonamethyl-4,8-dioxa-3,9-disilaundecane

There total 2 articles about (5S,6R)-5-[(S)-1-methoxy-2-(4-methoxybenzyloxy)ethyl]-2,2,3,3,6,9,9,10,10-nonamethyl-4,8-dioxa-3,9-disilaundecane 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: 75.0%

: 1262137-86-9
(2S,3S,4R)-3,5-bis[(tert-butyldimethylsilyl)oxy]-1-(4-methoxybenzyloxy)-4-methylpentan-2-ol

: 420-37-1
trimethoxonium tetrafluoroborate

: 1262137-87-0
(5S,6R)-5-[(S)-1-methoxy-2-(4-methoxybenzyloxy)ethyl]-2,2,3,3,6,9,9,10,10-nonamethyl-4,8-dioxa-3,9-disilaundecane

Guidance literature:: With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; In dichloromethane; at 20 ℃; for 12h; Inert atmosphere; Darkness;
DOI:10.1002/ejoc.201001097

Reference yield:

: 1262137-85-8
(2R,3S,4S)-3-[(tert-butyldimethylsilyl)oxy]-5-(4-methoxybenzyloxy)-2-methylpentane-1,4-diol

: 1262137-87-0
(5S,6R)-5-[(S)-1-methoxy-2-(4-methoxybenzyloxy)ethyl]-2,2,3,3,6,9,9,10,10-nonamethyl-4,8-dioxa-3,9-disilaundecane

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole / dichloromethane / 1 h / 0 °C / Inert atmosphere

2: N,N,N',N'-tetramethyl-1,8-diaminonaphthalene / dichloromethane / 12 h / 20 °C / Inert atmosphere; Darkness

With 1H-imidazole; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; In dichloromethane;
DOI:10.1002/ejoc.201001097