(2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane

Base Information

Chemical Name:(2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane
CAS No.:521274-25-9
Molecular Formula:C₅₁H₇₀O₅Si₂
Molecular Weight:819.285
Hs Code.:

Synonyms:(2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane

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Chemical Property of (2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane

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Technology Process of (2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane

There total 15 articles about (2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane 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:

: 118736-04-2
(4-(dimethoxymethyl)phenoxy)(tert-butyl)dimethylsilane

: 521274-24-8
(E)-(4R,5R)-8-Triisopropylsilanyloxy-5-(2-trityloxy-ethyl)-octa-1,6-diene-4,5-diol

: 521274-25-9
(2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane

Guidance literature:: With camphor-10-sulfonic acid; In N,N-dimethyl-formamide; at 50 ℃; for 0.666667h;
DOI:10.1021/ja0340679

Reference yield:

: 120743-99-9
p-[(tert-butyldimethylsilyl)oxy]benzaldehyde

: 521274-25-9
(2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane

Guidance literature:: Multi-step reaction with 2 steps

1: 6.82 g / CSA / methanol / 20 h / 23 °C

2: CSA / dimethylformamide / 0.67 h / 50 °C

With camphor-10-sulfonic acid; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/ja0340679

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 521274-25-9
(2R,4R,5R)-5-Allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-((E)-3-triisopropylsilanyloxy-propenyl)-4-(2-trityloxy-ethyl)-[1,3]dioxolane

Guidance literature:: Multi-step reaction with 3 steps

1: imidazole / CH₂Cl₂ / 0.5 h / 23 °C

2: 6.82 g / CSA / methanol / 20 h / 23 °C

3: CSA / dimethylformamide / 0.67 h / 50 °C

With 1H-imidazole; camphor-10-sulfonic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja0340679