C₂₀H₂₆O₂

Base Information

Chemical Name:C₂₀H₂₆O₂
CAS No.:952722-06-4
Molecular Formula:C₂₀H₂₆O₂
Molecular Weight:298.425
Hs Code.:

C<sub>20</sub>H<sub>26</sub>O<sub>2</sub>

Synonyms:C₂₀H₂₆O₂

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Chemical Property of C₂₀H₂₆O₂

Chemical Property:

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Technology Process of C₂₀H₂₆O₂

There total 13 articles about C₂₀H₂₆O₂ 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: 80.0%

: 952722-05-3
C₂₀H₂₈O₂

: 952722-06-4
C₂₀H₂₆O₂

Guidance literature:: With dipyridinium dichromate; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1016/j.tetasy.2007.07.007

Reference yield:

: 1036373-94-0
C₁₃H₁₈N₂O₃

: 952722-06-4
C₂₀H₂₆O₂

Guidance literature:: Multi-step reaction with 9 steps

1: Rh₂(OAc)4 / CH₂Cl₂

2: lithium aluminium hydride / diethyl ether / 1 h / 0 °C

3: 79 percent / pyridinium chlorochromate; silica gel / CH₂Cl₂ / 2 h / 20 °C

4: 81 percent / lithium; liq. ammonia / 2-methyl-propan-2-ol; tetrahydrofuran / 0.17 h

5: 93 percent / sodium borohydride / methanol / 0.17 h / 0 °C

6: 89 percent / sodium hydride; tetrabutylammonium iodide / tetrahydrofuran

7: 63 percent / selenium dioxide; acetic acid / 1.5 h / Heating

8: 86 percent / lithium / tetrahydrofuran / 1 h / sonication

9: 80 percent / PDC / CH₂Cl₂ / 3 h / 20 °C

With sodium tetrahydroborate; lithium aluminium tetrahydride; dipyridinium dichromate; selenium(IV) oxide; ammonia; silica gel; tetra-(n-butyl)ammonium iodide; lithium; sodium hydride; acetic acid; pyridinium chlorochromate; dirhodium tetraacetate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; tert-butyl alcohol; 8: Barbier reaction;
DOI:10.1016/j.tetasy.2007.07.007

Reference yield:

: 952722-00-8
C₁₂H₁₈N₂O

: 952722-06-4
C₂₀H₂₆O₂

Guidance literature:: Multi-step reaction with 6 steps

1: 61 percent / Rh₂(OAc)4*2H₂O / CH₂Cl₂ / 3 h / Heating

2: 93 percent / sodium borohydride / methanol / 0.17 h / 0 °C

3: 89 percent / sodium hydride; tetrabutylammonium iodide / tetrahydrofuran

4: 63 percent / selenium dioxide; acetic acid / 1.5 h / Heating

5: 86 percent / lithium / tetrahydrofuran / 1 h / sonication

6: 80 percent / PDC / CH₂Cl₂ / 3 h / 20 °C

With sodium tetrahydroborate; dipyridinium dichromate; selenium(IV) oxide; tetra-(n-butyl)ammonium iodide; lithium; sodium hydride; acetic acid; dirhodium tetracetate dihydrate; In tetrahydrofuran; methanol; dichloromethane; 5: Barbier reaction;
DOI:10.1016/j.tetasy.2007.07.007