C₁₉H₃₀O₅

Base Information

Chemical Name:C₁₉H₃₀O₅
CAS No.:1591927-94-4
Molecular Formula:C₁₉H₃₀O₅
Molecular Weight:338.444
Hs Code.:

C<sub>19</sub>H<sub>30</sub>O<sub>5</sub>

Synonyms:C₁₉H₃₀O₅

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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 C₁₉H₃₀O₅

Chemical Property:

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Technology Process of C₁₉H₃₀O₅

There total 9 articles about C₁₉H₃₀O₅ 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:

: C₃₅H₄₈O₅Si

: 1591927-94-4
C₁₉H₃₀O₅

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ol5008179

Reference yield:

: 1591927-49-9
C₃₂H₅₂O₄Si₂

: 1591927-94-4
C₁₉H₃₀O₅

Guidance literature:: Multi-step reaction with 7 steps

1: tetramethylammonium triacetoxyborohydride / acetonitrile; acetic acid / 24 h / -40 - -30 °C / Inert atmosphere

2: camphor-10-sulfonic acid / dichloromethane; methanol / 4 h / 0 - 20 °C / Inert atmosphere

3: camphor-10-sulfonic acid / dichloromethane; methanol / 2 h / 0 °C / Inert atmosphere

4: Proton-sponge / dichloromethane / 6 h / 0 - 20 °C / Inert atmosphere

5: diisobutylaluminium hydride / dichloromethane; toluene / -10 °C / Inert atmosphere

6: Dess-Martin periodane / dichloromethane; tert-butyl alcohol / 0 - 20 °C / Inert atmosphere

7: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 - 20 °C / Inert atmosphere

With camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; Dess-Martin periodane; tetramethylammonium triacetoxyborohydride; In tetrahydrofuran; methanol; dichloromethane; acetic acid; toluene; acetonitrile; tert-butyl alcohol;
DOI:10.1021/ol5008179

Reference yield:

: 206255-62-1
4-(tert-butyl-dimethyl-silanyloxy)-3,3-dimethyl-butan-2-one

: 1591927-94-4
C₁₉H₃₀O₅

Guidance literature:: Multi-step reaction with 9 steps

1: triethylamine / diethyl ether / 0 - 20 °C / Inert atmosphere

2: boron trifluoride diethyl etherate / dichloromethane / -95 - -78 °C / Inert atmosphere

3: tetramethylammonium triacetoxyborohydride / acetonitrile; acetic acid / 24 h / -40 - -30 °C / Inert atmosphere

4: camphor-10-sulfonic acid / dichloromethane; methanol / 4 h / 0 - 20 °C / Inert atmosphere

5: camphor-10-sulfonic acid / dichloromethane; methanol / 2 h / 0 °C / Inert atmosphere

6: Proton-sponge / dichloromethane / 6 h / 0 - 20 °C / Inert atmosphere

7: diisobutylaluminium hydride / dichloromethane; toluene / -10 °C / Inert atmosphere

8: Dess-Martin periodane / dichloromethane; tert-butyl alcohol / 0 - 20 °C / Inert atmosphere

9: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 - 20 °C / Inert atmosphere

With camphor-10-sulfonic acid; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; Dess-Martin periodane; triethylamine; tetramethylammonium triacetoxyborohydride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetic acid; toluene; acetonitrile; tert-butyl alcohol; 2: |Mukaiyama Aldol Addition;
DOI:10.1021/ol5008179