C₂₄H₃₁F₃O₈S

Base Information

Chemical Name:C₂₄H₃₁F₃O₈S
CAS No.:1335098-31-1
Molecular Formula:C₂₄H₃₁F₃O₈S
Molecular Weight:536.567
Hs Code.:

C<sub>24</sub>H<sub>31</sub>F<sub>3</sub>O<sub>8</sub>S

Synonyms:C₂₄H₃₁F₃O₈S

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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 C₂₄H₃₁F₃O₈S

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Technology Process of C₂₄H₃₁F₃O₈S

There total 10 articles about C₂₄H₃₁F₃O₈S 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: 57.0%

: 1335098-30-0
C₂₃H₃₂O₆

: 121287-02-3
N-(4-tert-butylphenyl)-1,1,1-trifluoro-N-[(trifluoromethyl)sulphonyl]methanesulphonamide

: 1335098-31-1
C₂₄H₃₁F₃O₈S

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 - 20 ℃; for 0.333333h; Inert atmosphere;
DOI:10.1002/anie.201103270

Reference yield:

: 1335098-29-7
C₂₄H₃₄O₇

: 1335098-31-1
C₂₄H₃₁F₃O₈S

Guidance literature:: Multi-step reaction with 3 steps

1: n-butyllithium / tetrahydrofuran; hexane / 0.42 h / -78 - 0 °C / Inert atmosphere

2: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 3 h / 110 °C / Inert atmosphere

3: lithium hexamethyldisilazane / tetrahydrofuran / 0.33 h / -78 - 20 °C / Inert atmosphere

With n-butyllithium; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; toluene;
DOI:10.1002/anie.201103270

Reference yield:

: 1335098-28-6
C₂₇H₄₄O₇Si

: 1335098-31-1
C₂₄H₃₁F₃O₈S

Guidance literature:: Multi-step reaction with 5 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1.5 h / 0 - 20 °C / Inert atmosphere

2: camphor-10-sulfonic acid / dichloromethane / 14 h / 0 - 20 °C / Inert atmosphere

3: n-butyllithium / tetrahydrofuran; hexane / 0.42 h / -78 - 0 °C / Inert atmosphere

4: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 3 h / 110 °C / Inert atmosphere

5: lithium hexamethyldisilazane / tetrahydrofuran / 0.33 h / -78 - 20 °C / Inert atmosphere

With n-butyllithium; 2,2'-azobis(isobutyronitrile); camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; tri-n-butyl-tin hydride; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; dichloromethane; toluene;
DOI:10.1002/anie.201103270