C₃₄H₄₅F₃N₂O₈

Base Information

Chemical Name:C₃₄H₄₅F₃N₂O₈
CAS No.:1391426-11-1
Molecular Formula:C₃₄H₄₅F₃N₂O₈
Molecular Weight:666.735
Hs Code.:

C<sub>34</sub>H<sub>45</sub>F<sub>3</sub>N<sub>2</sub>O<sub>8</sub>

Synonyms:

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Chemical Property of C₃₄H₄₅F₃N₂O₈

Chemical Property:

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Technology Process of C₃₄H₄₅F₃N₂O₈

There total 5 articles about C₃₄H₄₅F₃N₂O₈ 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:

: 1391426-05-3
(E,E)-2-nitro-4-farnesylpyrrole

: 1391426-11-1
C₃₄H₄₅F₃N₂O₈

Guidance literature:: Multi-step reaction with 3 steps

1: dmap / acetonitrile / 0.5 h / 20 °C

2: potassium osmate(VI) dihydrate; methanesulfonamide; potassium carbonate; potassium hexacyanoferrate(III) / water; tert-butyl alcohol / 24 h / 0 °C

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

With dmap; potassium osmate(VI) dihydrate; methanesulfonamide; potassium carbonate; triethylamine; potassium hexacyanoferrate(III); In dichloromethane; water; acetonitrile; tert-butyl alcohol;
DOI:10.1021/ol300954s

Reference yield:

: C₂₈H₄₉NSi

: 1391426-11-1
C₃₄H₄₅F₃N₂O₈

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C

1.2: 1 h / 0 °C

2.1: dmap / acetonitrile / 0.5 h / 20 °C

3.1: potassium osmate(VI) dihydrate; methanesulfonamide; potassium carbonate; potassium hexacyanoferrate(III) / water; tert-butyl alcohol / 24 h / 0 °C

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

With dmap; potassium osmate(VI) dihydrate; methanesulfonamide; tetrabutyl ammonium fluoride; potassium carbonate; triethylamine; potassium hexacyanoferrate(III); In tetrahydrofuran; dichloromethane; water; acetonitrile; tert-butyl alcohol;
DOI:10.1021/ol300954s

Reference yield:

: 24163-93-7,24163-94-8,56881-57-3,6874-67-5,28290-41-7
farnesyl bromide

: 1391426-11-1
C₃₄H₄₅F₃N₂O₈

Guidance literature:: Multi-step reaction with 5 steps

1.1: tert.-butyl lithium / tetrahydrofuran; pentane / 0.08 h / -78 °C

1.2: 4.08 h / -78 - -50 °C

2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C

2.2: 1 h / 0 °C

3.1: dmap / acetonitrile / 0.5 h / 20 °C

4.1: potassium osmate(VI) dihydrate; methanesulfonamide; potassium carbonate; potassium hexacyanoferrate(III) / water; tert-butyl alcohol / 24 h / 0 °C

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

With dmap; potassium osmate(VI) dihydrate; methanesulfonamide; tetrabutyl ammonium fluoride; tert.-butyl lithium; potassium carbonate; triethylamine; potassium hexacyanoferrate(III); In tetrahydrofuran; dichloromethane; water; acetonitrile; tert-butyl alcohol; pentane;
DOI:10.1021/ol300954s