C₂₆H₃₃NO₆

Base Information

Chemical Name:C₂₆H₃₃NO₆
CAS No.:1265173-11-2
Molecular Formula:C₂₆H₃₃NO₆
Molecular Weight:455.551
Hs Code.:

C<sub>26</sub>H<sub>33</sub>NO<sub>6</sub>

Synonyms:C₂₆H₃₃NO₆

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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 C₂₆H₃₃NO₆

Chemical Property:

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Technology Process of C₂₆H₃₃NO₆

There total 15 articles about C₂₆H₃₃NO₆ 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: 100.0%

: 1265173-09-8
C₂₉H₄₁NO₆Si

: 1265173-11-2
C₂₆H₃₃NO₆

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 0.166667h;
DOI:10.1002/asia.201000602

Reference yield: 57.0%

: 1265173-09-8
C₂₉H₄₁NO₆Si

: 1196704-26-3
C₂₅H₃₁NO₆

: 1265173-11-2
C₂₆H₃₃NO₆

Guidance literature:: With scandium tris(trifluoromethanesulfonate); In dichloromethane; water; at 40 ℃; for 72h;
DOI:10.1002/asia.201000602

Reference yield:

: 1265173-19-0
C₁₈H₂₆O₅

: 1265173-11-2
C₂₆H₃₃NO₆

Guidance literature:: Multi-step reaction with 14 steps

1.1: water; acetic acid / 48 h / 20 °C

2.1: dmap / pyridine / 24 h / 20 °C

3.1: acetic anhydride; dimethyl sulfoxide / 2 h / 50 °C

4.1: toluene / 4 h / -40 °C

5.1: magnesium / methanol / 2 h / 20 °C

6.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / 4 h / 20 °C

7.1: sodium hydride / tetrahydrofuran; hexane; mineral oil / 0.17 h / 0 °C

7.2: 0 - 20 °C

8.1: pyridine / dichloromethane / 2 h / 0 °C

9.1: diisobutylaluminium hydride / toluene / 0.5 h / -78 °C

10.1: dichloromethane / 1 h / 0 °C

11.1: sodium carbonate / tert-butylbenzene / 24 h / 170 °C

12.1: diisobutylaluminium hydride / toluene / 1 h / -78 °C

13.1: potassium carbonate / tetrahydrofuran; water / 3 h / 0 °C

14.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.17 h / 0 °C

With pyridine; dmap; tetrabutyl ammonium fluoride; sulfur trioxide pyridine complex; acetic anhydride; sodium hydride; diisobutylaluminium hydride; sodium carbonate; potassium carbonate; magnesium; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; pyridine; methanol; tert-butylbenzene; hexane; dichloromethane; water; acetic acid; toluene; mineral oil; 6.1: Swern oxidation / 7.2: Horner-Wadsworth-Emmons olefination / 11.1: Overman rearrangement;
DOI:10.1002/asia.201000602