N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

Base Information

Chemical Name:N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide
CAS No.:329796-53-4
Molecular Formula:C₂₄H₃₄N₂O₆SSi
Molecular Weight:506.695
Hs Code.:

<i>N</i>-{1-[1-benzyl-2-(<i>tert</i>-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

Synonyms:N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

Suppliers and Price of N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

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-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

There total 5 articles about N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide 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:

: 98-74-8
4-Nitrobenzenesulfonyl chloride

: 329796-49-8
2-{(S)-1-[(R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-isoindole-1,3-dione

: 329796-53-4
N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

Guidance literature:: 2-{(S)-1-[(R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-isoindole-1,3-dione; With methylamine; In ethanol; dichloromethane; at 23 ℃; for 0.25h;

4-Nitrobenzenesulfonyl chloride; With 2,4,6-trimethyl-pyridine; In dichloromethane; at 0 ℃; for 0.25h; Further stages.;
DOI:10.1021/ja0023377

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 329796-53-4
N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: Et₃N / CH₂Cl₂ / 8 h / 23 °C

2.1: triphenylphosphine; diethyl azodicarboxylate / tetrahydrofuran / 0.75 h / 23 °C

3.1: MeNH₂ / ethanol; CH₂Cl₂ / 0.25 h / 23 °C

3.2: 2,4,6-collidine / CH₂Cl₂ / 0.25 h / 0 °C

With triethylamine; triphenylphosphine; methylamine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/ja0023377

Reference yield:

: 329796-45-4
(2R,3R)-2-Benzyl-pent-4-ene-1,3-diol

: 329796-53-4
N-{1-[1-benzyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-allyloxy}-4-nitro-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: Et₃N / CH₂Cl₂ / 8 h / 23 °C

2.1: triphenylphosphine; diethyl azodicarboxylate / tetrahydrofuran / 0.75 h / 23 °C

3.1: MeNH₂ / ethanol; CH₂Cl₂ / 0.25 h / 23 °C

3.2: 2,4,6-collidine / CH₂Cl₂ / 0.25 h / 0 °C

With triethylamine; triphenylphosphine; methylamine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/ja0023377