ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate

Base Information

Chemical Name:ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate
CAS No.:1263870-43-4
Molecular Formula:C₂₂H₂₄FNO₄
Molecular Weight:385.435
Hs Code.:

Synonyms:ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate

Suppliers and Price of ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate

There total 5 articles about ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate 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: 70.0%

: 1263870-42-3
ethyl 3-((3-ethoxy-3-oxopropyl)(4-methoxybenzyl)amino)-2-(4-fluorophenyl)propanoate

: 1263870-43-4
ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield:

: 459-22-3
4-fluorophenylacetonitrile

: 1263870-43-4
ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / tetrahydrofuran / 0.25 h / -10 °C

1.2: -10 - 40 °C

2.1: hydrogen; sulfuric acid; acetic acid / palladium 10% on activated carbon / methanol / 18 h / 20 °C / 3677.86 Torr

3.1: ethanol / 18 h / 20 °C

4.1: potassium carbonate / acetone / 3 h / Reflux

5.1: potassium tert-butylate / tetrahydrofuran / 2 h / 20 °C

With sulfuric acid; potassium tert-butylate; hydrogen; sodium hydride; potassium carbonate; acetic acid; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; acetone;

Reference yield:

: 7054-58-2,15032-42-5
ethyl 2-cyano-2-(4-fluorophenyl)acetate

: 1263870-43-4
ethyl 5-(4-fluorophenyl)-1-(4-methoxybenzyl)-4-oxopiperidine-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen; sulfuric acid; acetic acid / palladium 10% on activated carbon / methanol / 18 h / 20 °C / 3677.86 Torr

2: ethanol / 18 h / 20 °C

3: potassium carbonate / acetone / 3 h / Reflux

4: potassium tert-butylate / tetrahydrofuran / 2 h / 20 °C

With sulfuric acid; potassium tert-butylate; hydrogen; potassium carbonate; acetic acid; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; acetone;