Benzenesulfonimidoyl chloride, N-(trimethylsilyl)-

Base Information

Chemical Name:Benzenesulfonimidoyl chloride, N-(trimethylsilyl)-
CAS No.:138937-41-4
Molecular Formula:C9H14ClNOSSi
Molecular Weight:247.821
Hs Code.:

Synonyms:

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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 Benzenesulfonimidoyl chloride, N-(trimethylsilyl)-

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Technology Process of Benzenesulfonimidoyl chloride, N-(trimethylsilyl)-

There total 4 articles about Benzenesulfonimidoyl chloride, N-(trimethylsilyl)- 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:

: 17865-14-4
N-(trimethylsilyl)benzene sulfonamide

: 138937-41-4
N-Trimethylsilylbenzenesulfonimidoyl Chloride

Guidance literature:: With dichlorotriphenyl-λ⁴-phosphane; triethylamine; In chloroform; at -78 - 0 ℃;

Reference yield:

: 98-10-2
benzenesulfonamide

: 138937-41-4
N-Trimethylsilylbenzenesulfonimidoyl Chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / Et₃N / benzene / Heating

2: Ph₃PCl₂, Et₃N / CHCl₃ / -78 - 0 °C

With dichlorotriphenyl-λ⁴-phosphane; triethylamine; In chloroform; benzene;

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 138937-41-4
N-Trimethylsilylbenzenesulfonimidoyl Chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 2 h / 90 - 120 °C / Inert atmosphere

2: thionyl chloride; triethylamine / toluene / 1 h / -78 °C / Inert atmosphere

With thionyl chloride; triethylamine; In toluene;
DOI:10.1021/ma302424u