4-[2-(3-Nitrophenoxy)ethyl]morpholine

Base Information

• Chemical Name: 4-[2-(3-Nitrophenoxy)ethyl]morpholine
• CAS No.: 182618-90-2
• Molecular Formula: C12H16 N2 O4
• Molecular Weight: 252.27
• DSSTox Substance ID: DTXSID10388164
• Wikidata: Q82182929
• Mol file: 182618-90-2.mol

Synonyms:4-[2-(3-nitrophenoxy)ethyl]morpholine;182618-90-2;4-(2-(3-Nitrophenoxy)ethyl)morpholine;Morpholine, 4-[2-(3-nitrophenoxy)ethyl]-;SCHEMBL1961763;DTXSID10388164;TZARIMLSZORYDL-UHFFFAOYSA-N;MFCD07368552;4-[2-(3-Nitro-phenoxy)-ethyl]-morpholine;FT-0764024;W-206302

Chemical Property of 4-[2-(3-Nitrophenoxy)ethyl]morpholine

Chemical Property:

• PSA: 67.52000
• LogP: 1.76690
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 252.11100700
• Heavy Atom Count: 18
• Complexity: 263

Purity/Quality:

98%min ^*data from raw suppliers

4-[2-(3-NITROPHENOXY)ETHYL]MORPHOLINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): R20/21/22-34:
• Hazard Codes: R20/21/22-34:
• Statements: 20/21/22-34
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1COCCN1CCOC2=CC=CC(=C2)[N+](=O)[O-]

Technology Process of 4-[2-(3-Nitrophenoxy)ethyl]morpholine

There total 2 articles about 4-[2-(3-Nitrophenoxy)ethyl]morpholine 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: 94.0%

meta-nitrophenol (554-84-7) + 4-(2-chloroethyl)morpholine hydrochride (3647-69-6) → 3-[2-(N-Morpholino)ethoxy]-1-nitrobenzene (182618-90-2)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 50 ℃; for 5h;

Reference yield:

N-(2-chlorethyl)morpholine (3240-94-6) + meta-nitrophenol (554-84-7) + caesium carbonate (534-17-8) → 3-[2-(N-Morpholino)ethoxy]-1-nitrobenzene (182618-90-2)

Guidance literature:

In 1,4-dioxane;

Reference yield: 56.0%

3-[2-(N-Morpholino)ethoxy]-1-nitrobenzene (182618-90-2) → 3-[2-(4-Morpholinyl)ethoxy]-benzenamine (112677-72-2)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In ethanol; at 20 ℃; for 1h; under 2585.81 Torr;

upstream raw materials:

N-(2-chlorethyl)morpholine

meta-nitrophenol

caesium carbonate

4-(2-chloroethyl)morpholine hydrochride

Downstream raw materials:

3-[2-(4-Morpholinyl)ethoxy]-benzenamine

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