4-Methoxy-3-[2-(piperidin-1-yl)ethoxy]aniline

Base Information

• Chemical Name: 4-Methoxy-3-[2-(piperidin-1-yl)ethoxy]aniline
• CAS No.: 170229-79-5
• Molecular Formula: C14H22N2O2
• Molecular Weight: 250.341
• DSSTox Substance ID: DTXSID10591999
• Wikidata: Q82485880
• Mol file: 170229-79-5.mol

Synonyms:170229-79-5;4-methoxy-3-(2-(piperidin-1-yl)ethoxy)benzenamine;4-Methoxy-3-[2-(piperidin-1-yl)ethoxy]aniline;SCHEMBL4023281;DTXSID10591999;KTSZNTFCOMFPLC-UHFFFAOYSA-N;DB-332387;3-(2-Piperidin-1-ylethoxy)-4-methoxyaniline;4-methoxy-3-(2-piperidin-1-ylethoxy)-phenylamine;4-Methoxy-3-(2-piperidin-1-yl-ethoxy)-phenylamine

Chemical Property of 4-Methoxy-3-[2-(piperidin-1-yl)ethoxy]aniline

Chemical Property:

• XLogP3: 2.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 250.168127949
• Heavy Atom Count: 18
• Complexity: 232

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C(C=C(C=C1)N)OCCN2CCCCC2

Technology Process of 4-Methoxy-3-[2-(piperidin-1-yl)ethoxy]aniline

There total 3 articles about 4-Methoxy-3-[2-(piperidin-1-yl)ethoxy]aniline 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:

1-[2-(2-methoxy-5-nitro-phenoxy)-ethyl]-piperidine (399579-80-7) → 4-methoxy-3-(2-piperidin-1-yl-ethoxy)-phenylamine (170229-79-5)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethanol; for 16h; under 760 Torr;

DOI:10.1016/j.bmcl.2005.08.004

Reference yield:

5-nitroguaiacol (636-93-1) → 4-methoxy-3-(2-piperidin-1-yl-ethoxy)-phenylamine (170229-79-5)

Guidance literature:

Multi-step reaction with 2 steps

1: aq. potassium carbonate / 1,2-dimethoxy-ethane / 24 h / 20 °C

2: H₂ / Pd/C / ethanol / 16 h / 760 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In 1,2-dimethoxyethane; ethanol;

DOI:10.1016/j.bmcl.2005.08.004

Reference yield:

N-chloroethylpiperidine hydrochloride (2008-75-5) → 4-methoxy-3-(2-piperidin-1-yl-ethoxy)-phenylamine (170229-79-5)

Guidance literature:

Multi-step reaction with 2 steps

1: aq. potassium carbonate / 1,2-dimethoxy-ethane / 24 h / 20 °C

2: H₂ / Pd/C / ethanol / 16 h / 760 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In 1,2-dimethoxyethane; ethanol;

DOI:10.1016/j.bmcl.2005.08.004

upstream raw materials:

1-[2-(2-methoxy-5-nitro-phenoxy)-ethyl]-piperidine

5-nitroguaiacol

N-chloroethylpiperidine hydrochloride

Downstream raw materials:

(2,2-dimethoxy-ethyl)-[4-methoxy-3-(2-piperidin-1-yl-ethoxy)-phenyl]-amine

C₂₂H₂₃FN₂O₄

5-(tert-butyl-dimethyl-silanyloxy)-2-(3,4-dichloro-phenyl)-pentanoic acid [4-methoxy-3-(2-piperidin-1-yl-ethoxy)-phenyl]-amide

2-(4-chloro-phenyl)-pent-4-enoic acid (4-methoxy-3-[2-(4-piperidin-1-yl)-ethoxy]-phenyl)-amide

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