N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide

Base Information

Chemical Name:N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide
CAS No.:817160-12-6
Molecular Formula:C₂₃H₃₄N₂O₇SSi
Molecular Weight:510.684
Hs Code.:

Synonyms:N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide

Suppliers and Price of N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide

There total 3 articles about N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide 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: 62.0%

: 30934-97-5
2,2-dimethoxyethanol

: 817160-10-4
N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-2-nitrobenzenesulfonamide

: 817160-12-6
N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at -20 - 30 ℃; for 21h;
DOI:10.1016/j.tet.2004.09.072

Reference yield:

: 68847-33-6
2-[(1,1,2,2-tetramethyl-1-silapropoxy)methyl]phenylamine

: 817160-12-6
N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / TEA / CH₂Cl₂ / 24 h / 30 °C

2: 62 percent / PPh₃; DIAD / tetrahydrofuran / 21 h / -20 - 30 °C

With di-isopropyl azodicarboxylate; TEA; triphenylphosphine; In tetrahydrofuran; dichloromethane; 2: Mitsunobu reaction;
DOI:10.1016/j.tet.2004.09.072

Reference yield:

: 1694-92-4
2-Nitrobenzenesulfonyl chloride

: 817160-12-6
N-[2-(tert-butyldimethylsilanyloxymethyl)phenyl]-N-(2,2-dimethoxyethyl)-2-nitrobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / TEA / CH₂Cl₂ / 24 h / 30 °C

2: 62 percent / PPh₃; DIAD / tetrahydrofuran / 21 h / -20 - 30 °C

With di-isopropyl azodicarboxylate; TEA; triphenylphosphine; In tetrahydrofuran; dichloromethane; 2: Mitsunobu reaction;
DOI:10.1016/j.tet.2004.09.072