C₂₀H₃₀O₆

Base Information

Chemical Name:C₂₀H₃₀O₆
CAS No.:1344072-92-9
Molecular Formula:C₂₀H₃₀O₆
Molecular Weight:366.455
Hs Code.:

C<sub>20</sub>H<sub>30</sub>O<sub>6</sub>

Synonyms:C₂₀H₃₀O₆

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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 C₂₀H₃₀O₆

Chemical Property:

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Technology Process of C₂₀H₃₀O₆

There total 11 articles about C₂₀H₃₀O₆ 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:

: 1344072-80-5
C₂₀H₂₈O₆

: 1344072-92-9
C₂₀H₃₀O₆

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; at -78 ℃; for 0.25h;
DOI:10.1021/ol202515x

Reference yield:

: 1344072-55-4
tert-butyl((2,2-dimethyl-1,3-dioxolan-4-ylidene)(methoxy)methoxy)dimethylsilane

: 1344072-92-9
C₂₀H₃₀O₆

Guidance literature:: Multi-step reaction with 3 steps

1: N-(p-toluenesulfonyl)-L-valine; borane-THF / tetrahydrofuran; dichloromethane / 0.17 h / -78 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.08 h / 0 °C

3: diisobutylaluminium hydride / dichloromethane / 0.25 h / -78 °C

With N-(p-toluenesulfonyl)-L-valine; borane-THF; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane; 1: Kiyooka Aldol Reaction;
DOI:10.1021/ol202515x

Reference yield:

: 89238-99-3
O-(4-methoxybenzyl)-trichloroacetimidate

: 1344072-92-9
C₂₀H₃₀O₆

Guidance literature:: Multi-step reaction with 9 steps

1.1: camphor-10-sulfonic acid / dichloromethane / 19 h / 20 °C

2.1: diisobutylaluminium hydride / dichloromethane / 1.5 h / -78 °C

3.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 - -45 °C

3.2: -45 - 20 °C

4.1: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C

4.2: 0 - 20 °C

5.1: diisobutylaluminium hydride / dichloromethane / 1 h / -78 °C

6.1: manganese(IV) oxide / dichloromethane / 0.5 h / 20 °C

7.1: N-(p-toluenesulfonyl)-L-valine; borane-THF / tetrahydrofuran; dichloromethane / 0.17 h / -78 °C

8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.08 h / 0 °C

9.1: diisobutylaluminium hydride / dichloromethane / 0.25 h / -78 °C

With N-(p-toluenesulfonyl)-L-valine; manganese(IV) oxide; borane-THF; oxalyl dichloride; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; sodium hydride; diisobutylaluminium hydride; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; mineral oil; 3.1: Swern oxidation / 3.2: Swern oxidation / 4.2: Wittig-Horner olefination / 7.1: Kiyooka Aldol Reaction;
DOI:10.1021/ol202515x