N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine

Base Information

Chemical Name:N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine
CAS No.:1264737-75-8
Molecular Formula:C₁₈H₁₈F₃NO₂S
Molecular Weight:369.408
Hs Code.:

Synonyms:N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine

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Chemical Property of N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine

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Technology Process of N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine

There total 7 articles about N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine 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: 51.0%

: 1264737-63-4
N-benzoyl-4-tertbutylphenyl sulfonimidoyl fluoride

: 81290-20-2
(trifluoromethyl)trimethylsilane

: 1264737-75-8
N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine

Guidance literature:: N-benzoyl-4-tertbutylphenyl sulfonimidoyl fluoride; (trifluoromethyl)trimethylsilane; In tetrahydrofuran; at 21 ℃; for 0.166667h; Inert atmosphere;

With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 21 ℃; for 12.5h; Inert atmosphere;
DOI:10.1021/ol103030w

Reference yield:

: 1264737-41-8
4-tert-butylbenzenesulfinic acid methyl ester

: 1264737-75-8
N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran

2.1: n-butyllithium / hexane

3.1: tert-butylhypochlorite / dichloromethane / 2 h / 0 °C / Inert atmosphere

4.1: potassium fluoride; 18-crown-6 ether / acetonitrile / 16 h / 21 °C / Inert atmosphere

5.1: tetrahydrofuran / 0.17 h / 21 °C / Inert atmosphere

5.2: 12.5 h / 21 °C / Inert atmosphere

With potassium fluoride; n-butyllithium; 18-crown-6 ether; tert-butylhypochlorite; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; dichloromethane; acetonitrile;
DOI:10.1021/ol103030w

Reference yield:

: C₁₇H₁₈ClNO₂S

: 1264737-75-8
N-benzoyl-4-tert-butylbenzene-trifluoromethyl sulfoximine

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium fluoride; 18-crown-6 ether / acetonitrile / 16 h / 21 °C / Inert atmosphere

2.1: tetrahydrofuran / 0.17 h / 21 °C / Inert atmosphere

2.2: 12.5 h / 21 °C / Inert atmosphere

With potassium fluoride; 18-crown-6 ether; In tetrahydrofuran; acetonitrile;
DOI:10.1021/ol103030w