N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide

Base Information

• Chemical Name: N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide
• CAS No.: 274902-58-8
• Molecular Formula: C₂₁H₂₅NO₄
• Molecular Weight: 355.434
• Mol file: 274902-58-8.mol

Synonyms:N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide

Chemical Property of N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

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Technology Process of N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide

There total 2 articles about N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide 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: 90.0%

2-(2-bromoethoxy)tetrahydropyran (17739-45-6,59146-56-4) + p-phenoxyacetanilide (6312-87-4) → N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide (274902-58-8)

Guidance literature:

With potassium hydroxide; In dimethyl sulfoxide; at 20 ℃;

DOI:10.1021/jm9905007

Reference yield:

4-phenoxyanilin (139-59-3) → N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide (274902-58-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 98 percent / pyridine / 20 °C

2: 90 percent / KOH / dimethylsulfoxide / 20 °C

With pyridine; potassium hydroxide; In dimethyl sulfoxide; 1: Acetylation / 2: Alkylation;

DOI:10.1021/jm9905007

Reference yield:

N-(4-phenoxy-phenyl)-N-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-acetamide (274902-58-8) → N-acetyl-(4-phenoxyphenyl)-2-chloroethylamine (274902-60-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 73 percent / pyridinium 4-tolunensulfonate / methanol / 96 h / 20 °C

2: 51 percent / Ph₃P; Cl₄C / acetonitrile / 20 °C

With tetrachloromethane; pyridinium p-toluenesulfonate; triphenylphosphine; In methanol; acetonitrile; 1: Hydrolysis / 2: Chlorination;

DOI:10.1021/jm9905007

upstream raw materials:

2-(2-bromoethoxy)tetrahydropyran

p-phenoxyacetanilide

4-phenoxyanilin

Downstream raw materials:

N-acetyl-(4-phenoxyphenyl)-2-chloroethylamine