{(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane

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Chemical Name:{(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane
CAS No.:241155-46-4
Molecular Formula:C₄₈H₅₆O₅Si
Molecular Weight:741.055
Hs Code.:

Synonyms:{(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane

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Chemical Property of {(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane

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Technology Process of {(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane

There total 11 articles about {(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane 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%

: 1779-49-3
Methyltriphenylphosphonium bromide

: 241155-45-3
(E)-(5R,6S)-1-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-7-trityloxy-hept-3-en-2-one

: 241155-46-4
{(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane

Guidance literature:: With n-butyllithium; at -20 - 20 ℃; for 12h;
DOI:10.1055/s-1999-2743

Reference yield:

: 19810-31-2
Benzyloxyacetyl chloride

: 241155-46-4
{(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / n-BuLi / tetrahydrofuran / -78 - 50 °C

2: LiCl, i-Pr₂NEt / acetonitrile / 30 h / Ambient temperature

3: 79 percent / n-BuLi / 12 h / -20 - 20 °C

With n-butyllithium; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; acetonitrile;
DOI:10.1055/s-1999-2743

Reference yield:

: 30379-55-6
benzyloxyacetic acid

: 241155-46-4
{(E)-(R)-4-Benzyloxymethyl-1-[(S)-1-(4-methoxy-benzyloxy)-2-trityloxy-ethyl]-penta-2,4-dienyloxy}-tert-butyl-dimethyl-silane

Guidance literature:: Multi-step reaction with 4 steps

1: SOCl₂ / methanol / 12 h / -20 - 20 °C

2: 96 percent / n-BuLi / tetrahydrofuran / -78 - 50 °C

3: LiCl, i-Pr₂NEt / acetonitrile / 30 h / Ambient temperature

4: 79 percent / n-BuLi / 12 h / -20 - 20 °C

With n-butyllithium; thionyl chloride; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1055/s-1999-2743