3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole

Base Information

• Chemical Name: 3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole
• CAS No.: 155880-40-3
• Molecular Formula: C₃₀H₂₆N₂O₄S₂
• Molecular Weight: 542.679
• Mol file: 155880-40-3.mol

Synonyms:3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole

Chemical Property of 3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole

There total 2 articles about 3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole 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: 77.0%

N-(benzylidene)-p-methylbenzenesulfonamide (51608-60-7) + 3-ethenyl-1-phenylsulfonyl-1H-indole (82980-12-9) → 3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole (155880-40-3)

Guidance literature:

With lithium diisopropyl amide; In tetrahydrofuran; hexane; 1.) -78 to 0 deg C, 45 min; 25 deg C, 3 h, 2.) -78 deg C, 5 min; -78 to 0 deg C;

DOI:10.1021/jo00090a046

Reference yield:

1-(phenylsulfonyl)indole-3-carbaldehyde (80360-20-9) → 3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole (155880-40-3)

Guidance literature:

Multi-step reaction with 2 steps

2: 77 percent / LDA / hexane; tetrahydrofuran / 1.) -78 to 0 deg C, 45 min; 25 deg C, 3 h, 2.) -78 deg C, 5 min; -78 to 0 deg C

With lithium diisopropyl amide; In tetrahydrofuran; hexane;

DOI:10.1021/jo00090a046

Reference yield: 98.0%

methanol (67-56-1) + 3-Ethenyl-1-(benzenesulfonyl)-2-methyl>indole (155880-40-3) → 3-(2-Bromo-1-methoxyethyl)-1-(benzenesulfonyl)-2-methyl>indole (155880-44-7)

Guidance literature:

With bromine; In tetrachloromethane; dichloromethane; at 25 ℃; for 3h;

DOI:10.1021/jo00090a046

upstream raw materials:

N-(benzylidene)-p-methylbenzenesulfonamide

3-ethenyl-1-phenylsulfonyl-1H-indole

1-(phenylsulfonyl)indole-3-carbaldehyde

Downstream raw materials:

3-(2-Bromo-1-methoxyethyl)-1-(benzenesulfonyl)-2-methyl>indole

1-phenyl-9H-pyrido[3,4-b]indole

1-Phenyl-2-(p-toluenesulfonyl)-1,2-dihydro-β-carboline