N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide

Base Information

• Chemical Name: N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide
• CAS No.: 908131-24-8
• Molecular Formula: C₁₆H₁₈ClNO₃S
• Molecular Weight: 339.843
• Mol file: 908131-24-8.mol

Synonyms:N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide

Chemical Property of N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide

There total 5 articles about N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-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: 100.0%

3-(4-chloro-phenyl)-3-(toluene-4-sulfonylamino)-propionic acid tert-butyl ester (908131-19-1) → N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide (908131-24-8)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 1h;

DOI:10.1016/j.tetlet.2006.05.058

Reference yield:

3-(4-chloro-phenyl)-3-(toluene-4-sulfonylamino)-propionic acid ethyl ester → N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide (908131-24-8)

Guidance literature:

With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 5h; Inert atmosphere;

DOI:10.1021/acs.orglett.8b01394

Reference yield:

N-(p-chlorobenzylidene)-p-toluenesulfonamide (3157-65-1) → N-[1-(4-chloro-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide (908131-24-8)

Guidance literature:

Multi-step reaction with 2 steps

1.1: LDA / tetrahydrofuran / 1 h / -78 °C

1.2: 100 percent / tetrahydrofuran / 2 h / -78 °C

2.1: 100 percent / LAH / tetrahydrofuran / 1 h / 0 - 20 °C

With lithium aluminium tetrahydride; lithium diisopropyl amide; In tetrahydrofuran;

DOI:10.1016/j.tetlet.2006.05.058

upstream raw materials:

3-(4-chloro-phenyl)-3-(toluene-4-sulfonylamino)-propionic acid tert-butyl ester

N-(p-chlorobenzylidene)-p-toluenesulfonamide

4-chlorobenzaldehyde

toluene-4-sulfonamide

Downstream raw materials:

4-(4-chloro-phenyl)-2-methyl-1-(toluene-4-sulfonyl)-1,4,5,6-tetrahydro-pyrimidine

2-(4-chlorophenyl)-1-(4-toluenesulfonyl)azetidine