C₂₉H₄₂O₆

Base Information

Chemical Name:C₂₉H₄₂O₆
CAS No.:1609652-03-0
Molecular Formula:C₂₉H₄₂O₆
Molecular Weight:486.649
Hs Code.:

C<sub>29</sub>H<sub>42</sub>O<sub>6</sub>

Synonyms:C₂₉H₄₂O₆

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Chemical Property of C₂₉H₄₂O₆

Chemical Property:

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Technology Process of C₂₉H₄₂O₆

There total 15 articles about C₂₉H₄₂O₆ 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:

: 1609652-02-9
(3R,6S,7R)-3-(benzyloxy)-7-((4-methoxybenzyl)oxy)-6-(methoxymethoxy)dodecan-1-ol

: 1609652-03-0
C₂₉H₄₂O₆

Guidance literature:: With Dess-Martin periodane; In dichloromethane; at 0 - 20 ℃; for 1h;
DOI:10.1039/c4ob00323c

Reference yield:

: 1609652-00-7
(3R,6S,7R)-7-((4-methoxybenzyl)oxy)-6-(methoxymethoxy)dodecane-1,3-diol

: 1609652-03-0
C₂₉H₄₂O₆

Guidance literature:: Multi-step reaction with 3 steps

1: pyridinium p-toluenesulfonate / dichloromethane / 0 °C

2: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -20 °C

3: Dess-Martin periodane / dichloromethane / 1 h / 0 - 20 °C

With pyridinium p-toluenesulfonate; diisobutylaluminium hydride; Dess-Martin periodane; In dichloromethane; toluene;
DOI:10.1039/c4ob00323c

Reference yield:

: 132015-83-9
((4S,5R)-2,2-dimethyl-5-propyl-1,3-dioxolan-4-yl)methanol

: 1609652-03-0
C₂₉H₄₂O₆

Guidance literature:: Multi-step reaction with 14 steps

1.1: dmap; triethylamine / dichloromethane / 0 - 20 °C

2.1: toluene-4-sulfonic acid / methanol / 0 - 20 °C

3.1: potassium carbonate / methanol / 2 h / 0 °C

4.1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 0 °C

4.2: 0 - 20 °C

5.1: copper(I) bromide / tetrahydrofuran; diethyl ether / 0 °C

6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 8 h / 0 - 20 °C

7.1: ozone / dichloromethane / -78 °C / Inert atmosphere

8.1: benzene / 2 h / 20 °C

9.1: diisobutylaluminium hydride / dichloromethane; toluene / 20 °C / Cooling

10.1: titanium(IV) isopropylate; D-(-)-diisopropyl tartrate / dichloromethane / 0.5 h / -20 °C / Molecular sieve

10.2: 3 h / -20 °C

11.1: sodium bis(2-methoxyethoxy)aluminium dihydride / tetrahydrofuran; toluene / 2.5 h / 0 °C

12.1: pyridinium p-toluenesulfonate / dichloromethane / 0 °C

13.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -20 °C

14.1: Dess-Martin periodane / dichloromethane / 1 h / 0 - 20 °C

With titanium(IV) isopropylate; dmap; pyridinium p-toluenesulfonate; sodium hydride; diisobutylaluminium hydride; potassium carbonate; D-(-)-diisopropyl tartrate; Dess-Martin periodane; toluene-4-sulfonic acid; ozone; triethylamine; N-ethyl-N,N-diisopropylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; copper(I) bromide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; toluene; mineral oil; benzene; 8.1: |Wittig Olefination / 10.1: |Sharpless Asymmetric Epoxidation;
DOI:10.1039/c4ob00323c