(3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane

Base Information

• Chemical Name: (3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane
• CAS No.: 171013-49-3
• Molecular Formula: C₂₉H₂₉NO₅SSi
• Molecular Weight: 531.704
• Mol file: 171013-49-3.mol

Synonyms:(3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane

Chemical Property of (3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane

There total 6 articles about (3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane 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: 95.0%

tert-butylchlorodiphenylsilane (58479-61-1) + 3-Benzenesulfonylmethyl-5-nitro-phenol (180628-76-6) → (3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane (171013-49-3)

Guidance literature:

With 1H-imidazole;

DOI:10.1021/ja00148a034

Reference yield:

3-hydroxy-5-nitrobenzoic acid (78238-14-9) → (3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane (171013-49-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 60 percent / BH₃*THF / tetrahydrofuran / 15 h / Ambient temperature

2: 85 percent / CBr₄, Ph₃P / tetrahydrofuran / 2 h / 0 - 20 °C

3: 75 percent / dimethylformamide / 15 h / 60 °C

4: 95 percent / imidazole / dimethylformamide / 24 h / Ambient temperature

With 1H-imidazole; borane-THF; carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; N,N-dimethyl-formamide;

DOI:10.1021/ja961401a

Reference yield:

3-hydroxy-5-nitrobenzyl alcohol (180628-74-4) → (3-Benzenesulfonylmethyl-5-nitro-phenoxy)-tert-butyl-diphenyl-silane (171013-49-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 85 percent / CBr₄, Ph₃P / tetrahydrofuran / 2 h / 0 - 20 °C

2: 75 percent / dimethylformamide / 15 h / 60 °C

3: 95 percent / imidazole / dimethylformamide / 24 h / Ambient temperature

With 1H-imidazole; carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; N,N-dimethyl-formamide;

DOI:10.1021/ja961401a

upstream raw materials:

tert-butylchlorodiphenylsilane

3-Benzenesulfonylmethyl-5-nitro-phenol

3-hydroxy-5-nitrobenzoic acid

3-hydroxy-5-nitrobenzyl alcohol

Downstream raw materials:

C₅₆H₈₈Cl₃NO₈Si₃