S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine

Base Information

Chemical Name:S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine
CAS No.:181268-60-0
Molecular Formula:C₂₃H₃₅NO₃S₂Si
Molecular Weight:465.753
Hs Code.:

Synonyms:S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine

Suppliers and Price of S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine

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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 S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine

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Technology Process of S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine

There total 3 articles about S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)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: 75.0%

: 917-54-4
methyllithium

: 181268-53-1
S-Phenyl-S-((E)-1-trimethylsilylhex-1-enyl)-N-(toluene-p-sulfonyl)sulfoximine

: 181268-60-0
S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine

Guidance literature:: In tetrahydrofuran; at -78 ℃; for 0.5h;
DOI:10.1039/p19960001673

Reference yield:

: 147383-20-8
S-((E)-prop-1-enyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximide

: 181268-60-0
S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / 1.) MeLi / tetrahydrofuran; diethyl ether / 1.) -78 deg C, 30 min, 2.) -78 deg C, 20 min.

2: 76 percent / 1.) CuI / diethyl ether / 1.) -30 deg C, 30 min, 2.) 0 deg C, 75 min; r.t. 30 min

With copper(l) iodide; methyllithium; In tetrahydrofuran; diethyl ether;
DOI:10.1039/p19960001673

Reference yield:

: 181268-42-8
(S)-(+)-(E)-S-(hex-1-enyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximine

: 181268-60-0
S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / 1.) BuLi / tetrahydrofuran; diethyl ether / 1.) -78 deg C, 30 min, 2.) -78 deg C, 20 min.

2: 75 percent / tetrahydrofuran / 0.5 h / -78 °C

With n-butyllithium; In tetrahydrofuran; diethyl ether;
DOI:10.1039/p19960001673