(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal

Base Information

Chemical Name:(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal
CAS No.:303158-53-4
Molecular Formula:C₂₄H₃₂O₄Si
Molecular Weight:412.601
Hs Code.:

Synonyms:(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal

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Technology Process of (E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal

There total 7 articles about (E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal 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: 90.0%

: 303158-66-9
(E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol

: 303158-53-4
(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal

Guidance literature:: With sodium periodate; sodium hydrogencarbonate; In dichloromethane;
DOI:10.1021/ol0063656

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 303158-53-4
(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal

Guidance literature:: Multi-step reaction with 7 steps

1.1: 98 percent / imidazole / dimethylformamide

2.1: CH₂Cl₂

2.2: 98 percent / Me₂S

3.1: 96 percent / toluene / Heating

4.1: 95 percent / DIBAL / CH₂Cl₂ / 0 °C

5.1: 94 percent / i-Pr₂NEt / CH₂Cl₂

6.1: 89 percent / aq. AcOH

7.1: 90 percent / NaIO₄; NaHCO₃ / CH₂Cl₂

With 1H-imidazole; sodium periodate; diisobutylaluminium hydride; sodium hydrogencarbonate; acetic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; toluene; 1.1: silylation / 2.1: ozonation / 2.2: Reduction / 3.1: Wittig olefination / 4.1: Reduction / 5.1: Alkylation / 6.1: Hydrolysis / 7.1: Oxidation;
DOI:10.1021/ol0063656

Reference yield:

: 209479-86-7
(2R,3R)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol

: 303158-53-4
(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-5-methoxymethoxy-4-methyl-pent-3-enal

Guidance literature:: Multi-step reaction with 6 steps

1.1: CH₂Cl₂

1.2: 98 percent / Me₂S

2.1: 96 percent / toluene / Heating

3.1: 95 percent / DIBAL / CH₂Cl₂ / 0 °C

4.1: 94 percent / i-Pr₂NEt / CH₂Cl₂

5.1: 89 percent / aq. AcOH

6.1: 90 percent / NaIO₄; NaHCO₃ / CH₂Cl₂

With sodium periodate; diisobutylaluminium hydride; sodium hydrogencarbonate; acetic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane; toluene; 1.1: ozonation / 1.2: Reduction / 2.1: Wittig olefination / 3.1: Reduction / 4.1: Alkylation / 5.1: Hydrolysis / 6.1: Oxidation;
DOI:10.1021/ol0063656