1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone

Base Information

• Chemical Name: 1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone
• CAS No.: 117023-60-6
• Molecular Formula: C₃₀H₃₃F₂NO₃
• Molecular Weight: 493.594

Synonyms:1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone

Chemical Property of 1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone

Chemical Property:

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Technology Process of 1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone

There total 5 articles about 1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone 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: 76.0%

1-[4-(3-chloro-propoxy)-phenyl]-propan-1-one (65976-48-9) + 1,1-bis(4-fluorophenyl)-1-(4-piperidinyl)methanol (60284-98-2) → 1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone (117023-60-6)

Guidance literature:

With sodium carbonate; potassium iodide; In butan-1-ol; Heating;

DOI:10.1021/jm00121a022

Reference yield:

N-benzyl isonipecotic acid ethyl ester (24228-40-8) → 1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone (117023-60-6)

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: 76 percent / Na₂CO₃, KI / butan-1-ol / Heating

With hydrogen; sodium carbonate; magnesium; potassium iodide; palladium on activated charcoal; In ethanol; butan-1-ol;

DOI:10.1021/jm00121a022

Reference yield:

α,α-bis-(4-fluorophenyl)-1-(phenylmethyl)-4-piperidinemethanol (111627-25-9) → 1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]phenyl]-1-propanone (117023-60-6)

Guidance literature:

Multi-step reaction with 2 steps

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

2: 76 percent / Na₂CO₃, KI / butan-1-ol / Heating

With hydrogen; sodium carbonate; potassium iodide; palladium on activated charcoal; In ethanol; butan-1-ol;

DOI:10.1021/jm00121a022

upstream raw materials:

1-[4-(3-chloro-propoxy)-phenyl]-propan-1-one

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

N-benzyl isonipecotic acid ethyl ester

α,α-bis-(4-fluorophenyl)-1-(phenylmethyl)-4-piperidinemethanol

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