N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide

Base Information

Chemical Name:N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide
CAS No.:1159281-95-4
Molecular Formula:C₂₅H₃₀N₂O₅SSi
Molecular Weight:498.675
Hs Code.:

Synonyms:N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide

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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 N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide

Chemical Property:

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Technology Process of N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide

There total 1 articles about N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide 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:

: 58032-84-1
(3-nitrophenyl)methanesulfonyl chloride

: 91578-89-1
2-((tert-butyldiphenylsilyl)oxy)ethanamine

: 1159281-95-4
N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃;

Reference yield:

: 1159281-95-4
N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide

: 1159281-96-5
C-(3-aminophenyl)-N-[2-(tert-butyldiphenylsilanyloxy)-ethyl]methanesulfonamide

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; under 750.075 Torr;

Reference yield:

: 1159281-95-4
N-[2-(tert-butyldiphenyl-silanyloxy)ethyl]-C-(3-nitrophenyl)methanesulfonamide

: 1073485-64-9
C-(3-amino-phenyl)-N-(2-hydroxy-ethyl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / methanol / 750.08 Torr / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With tetrabutyl ammonium fluoride; hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; methanol;