1-(4-Aminophenoxy)-3-(dimethylamino)propan-2-ol

Base Information

• Chemical Name: 1-(4-Aminophenoxy)-3-(dimethylamino)propan-2-ol
• CAS No.: 260045-60-1
• Molecular Formula: C11H18N2O2
• Molecular Weight: 210.276
• European Community (EC) Number: 838-643-1
• Mol file: 260045-60-1.mol

Synonyms:260045-60-1;1-(4-Aminophenoxy)-3-(dimethylamino)propan-2-ol;4-[3-N,N-(dimethyl)amino-2-hydroxypropoxy]aniline;SCHEMBL188449;BOYVZXJHUROLHZ-UHFFFAOYSA-N;AKOS004123447;EN300-57297;1-(4-Amino-phenoxy)-3-dimethylamino-propan-2-ol;Z404979750

Chemical Property of 1-(4-Aminophenoxy)-3-(dimethylamino)propan-2-ol

Chemical Property:

• XLogP3: 0.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 210.136827821
• Heavy Atom Count: 15
• Complexity: 168

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C)CC(COC1=CC=C(C=C1)N)O

Technology Process of 1-(4-Aminophenoxy)-3-(dimethylamino)propan-2-ol

There total 4 articles about 1-(4-Aminophenoxy)-3-(dimethylamino)propan-2-ol 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: 72.4%

3-(N,N-dimethyl)amino-2-hydroxy-1-(4-nitrophenoxy)propane (260045-39-4) → 4-[3-N,N-(dimethyl)amino-2-hydroxypropoxy]aniline (260045-60-1)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethanol;

DOI:10.1016/S0960-894X(03)00638-3

Reference yield:

4-nitro-phenol (100-02-7,78813-13-5,89830-32-0) → 4-[3-N,N-(dimethyl)amino-2-hydroxypropoxy]aniline (260045-60-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 78 percent / K₂CO₃; Bu₄Br / 100 °C

2: 90 percent / methanol; dimethylformamide / 20 °C

3: 72 percent / H₂ / Pd/C / ethanol

With hydrogen; potassium carbonate; palladium on activated charcoal; In methanol; ethanol; N,N-dimethyl-formamide;

DOI:10.1016/S0960-894X(03)00638-3

Reference yield:

4-nitrophenyl 2-oxiranylmethyl ether (125228-75-3) → 4-[3-N,N-(dimethyl)amino-2-hydroxypropoxy]aniline (260045-60-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / methanol; dimethylformamide / 20 °C

2: 72 percent / H₂ / Pd/C / ethanol

With hydrogen; palladium on activated charcoal; In methanol; ethanol; N,N-dimethyl-formamide;

DOI:10.1016/S0960-894X(03)00638-3

upstream raw materials:

3-(N,N-dimethyl)amino-2-hydroxy-1-(4-nitrophenoxy)propane

4-nitro-phenol

4-nitrophenyl 2-oxiranylmethyl ether

Downstream raw materials:

4-(2-bromo4-methylphenoxy)-6-{4-[3-(N,N-dimethyl)amino-2-hydroxypropoxy]anilino}pyrimidine

N-[4-(3-dimethylamino-2-hydroxy-propoxy)-phenyl]-guanidine