2-[(Toluene-4-sulfonyl)-(triphenyl-λ⁵-phosphanylidene)-methyl]-2H-indazole

Base Information

• Chemical Name: 2-[(Toluene-4-sulfonyl)-(triphenyl-λ⁵-phosphanylidene)-methyl]-2H-indazole
• CAS No.: 101246-40-6
• Molecular Formula: C₃₃H₂₇N₂O₂PS
• Molecular Weight: 546.629
• Mol file: 101246-40-6.mol

Synonyms:2-[(Toluene-4-sulfonyl)-(triphenyl-λ⁵-phosphanylidene)-methyl]-2H-indazole

Chemical Property of 2-[(Toluene-4-sulfonyl)-(triphenyl-λ⁵-phosphanylidene)-methyl]-2H-indazole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-[(Toluene-4-sulfonyl)-(triphenyl-λ⁵-phosphanylidene)-methyl]-2H-indazole

There total 8 articles about 2-[(Toluene-4-sulfonyl)-(triphenyl-λ⁵-phosphanylidene)-methyl]-2H-indazole 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: 60.0%

C39H32N3O3PS (101246-31-5) → 2-[(Toluene-4-sulfonyl)-(triphenyl-λ5-phosphanylidene)-methyl]-2H-indazole (101246-40-6)

Guidance literature:

In toluene; at 80 ℃; for 10h;

DOI:10.1016/S0040-4020(01)96646-3

Reference yield:

2-formylphenylazo(methoxycarbonyl)methylenetriphenylphosphorane (70736-32-2) → 2-[(Toluene-4-sulfonyl)-(triphenyl-λ5-phosphanylidene)-methyl]-2H-indazole (101246-40-6)

Guidance literature:

Multi-step reaction with 5 steps

1: 88 percent / NaHCO₃ / ethanol / 3 h / 50 °C

2: toluene / 5 h / 110 °C

3: 86 percent / Et₃N / acetonitrile

4: 93 percent / ethanol / 3 h / 50 °C

5: 60 percent / toluene / 10 h / 80 °C

With sodium hydrogencarbonate; triethylamine; In ethanol; toluene; acetonitrile;

DOI:10.1016/S0040-4020(01)96646-3

Reference yield:

1-chloro-1-p.toluenesulphonylacetone (101246-34-8) → 2-[(Toluene-4-sulfonyl)-(triphenyl-λ5-phosphanylidene)-methyl]-2H-indazole (101246-40-6)

Guidance literature:

Multi-step reaction with 4 steps

1: 1.) HNO₂

2: 86 percent / Et₃N / acetonitrile

3: 93 percent / ethanol / 3 h / 50 °C

4: 60 percent / toluene / 10 h / 80 °C

With cis-nitrous acid; triethylamine; In ethanol; toluene; acetonitrile;

DOI:10.1016/S0040-4020(01)96646-3

upstream raw materials:

C₃₉H₃₂N₃O₃PS

2-formylphenylazo(methoxycarbonyl)methylenetriphenylphosphorane

1-chloro-1-p.toluenesulphonylacetone

o-aminobenzaldehyde