[4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester

Base Information

• Chemical Name: [4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester
• CAS No.: 117023-74-2
• Molecular Formula: C₃₀H₃₃F₂NO₄
• Molecular Weight: 509.593
• Mol file: 117023-74-2.mol

Synonyms:[4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester

Chemical Property of [4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester

There total 5 articles about [4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester 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: 43.0%

methyl [4-(3-chloropropoxy)phenyl]acetate (69182-96-3) + 1,1-bis(4-fluorophenyl)-1-(4-piperidinyl)methanol (60284-98-2) → [4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester (117023-74-2)

Guidance literature:

With sodium carbonate; potassium iodide; In N,N-dimethyl-formamide; Heating;

DOI:10.1021/jm00121a022

Reference yield:

N-benzyl isonipecotic acid ethyl ester (24228-40-8) → [4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester (117023-74-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 1) Mg / 1) THF, reflux, 15 min.; 2) THF, room temperature, overnight

2: 92 percent / H₂ / 5percent Pd/C / ethanol / 48 h / 70 °C / 2585.7 Torr

3: 43 percent / Na₂CO₃, KI / dimethylformamide / Heating

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

DOI:10.1021/jm00121a022

Reference yield:

α,α-bis-(4-fluorophenyl)-1-(phenylmethyl)-4-piperidinemethanol (111627-25-9) → [4-(3-{4-[Bis-(4-fluoro-phenyl)-hydroxy-methyl]-piperidin-1-yl}-propoxy)-phenyl]-acetic acid methyl ester (117023-74-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 92 percent / H₂ / 5percent Pd/C / ethanol / 48 h / 70 °C / 2585.7 Torr

2: 43 percent / Na₂CO₃, KI / dimethylformamide / Heating

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

DOI:10.1021/jm00121a022

upstream raw materials:

methyl [4-(3-chloropropoxy)phenyl]acetate

1,1-bis(4-fluorophenyl)-1-(4-piperidinyl)methanol

Methyl 4-hydroxyphenylacetate

N-benzyl isonipecotic acid ethyl ester

Downstream raw materials:

4-<3-<4--1-piperidinyl>propoxy>benzeneacetic acid