3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine

Base Information

• Chemical Name: 3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine
• CAS No.: 64819-94-9
• Molecular Formula: C₂₂H₃₄N₄O₅S₂
• Molecular Weight: 498.668
• Mol file: 64819-94-9.mol

Synonyms:3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine

Chemical Property of 3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine

There total 4 articles about 3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine 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: 82.0%

3,9-di(p-toluenesulfonyl)-1,11-di(p-toluenesulfonyloxy)-6-oxa-3,9-diazaundecane (76980-39-7) → 3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine (64819-94-9)

Guidance literature:

Gabriel reaction;

DOI:10.1021/ja00395a077

Reference yield:

N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide (14316-14-4) → 3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine (64819-94-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 65 percent / K₂CO₃ / dimethylformamide / 24 h / 70 °C

2: 93 percent / pyridine / 0 °C

With potassium carbonate; In pyridine; N,N-dimethyl-formamide;

DOI:10.1002/hlca.19830660426

Reference yield:

N,N'-di(para-toluensulfonyl)-3,9-diaza-6-oxaundecane-1,11-diol (50977-94-1) → 3,9-di(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine (64819-94-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 93 percent / pyridine / 0 °C

In pyridine;

DOI:10.1002/hlca.19830660426

upstream raw materials:

3,9-di(p-toluenesulfonyl)-1,11-di(p-toluenesulfonyloxy)-6-oxa-3,9-diazaundecane

N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide

N,N'-di(para-toluensulfonyl)-3,9-diaza-6-oxaundecane-1,11-diol

Downstream raw materials:

4,7,13,16,22,25-hexa(p-toluenesulfonyl)-1,10,19-trioxa-4,7,13,16,22,25-hexaazacycloheptaeicosane

4,10,16,22,27,33-hexakis-(toluene-4-sulfonyl)-7,19,30-trioxa-1,4,10,13,16,22,27,33-octaaza-bicyclo[11.11.11]pentatriacontane-2,12-dione

4,10,16,22-tetrakis(p-tolylsulfonyl)1,13-dioxa-4,7,10,16,19,22-hexaazacyclotetracosane

N,N',3,9-tetra(p-toluenesulfonyl)-6-oxa-3,9-diazaundecane-1,11-diamine