ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate

Base Information

Chemical Name:ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate
CAS No.:439944-55-5
Molecular Formula:C₂₅H₂₉NO₅
Molecular Weight:423.509
Hs Code.:

Synonyms:ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate

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Chemical Property of ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate

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Technology Process of ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate

There total 3 articles about ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate 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: 60.0%

: 2567-29-5
p-phenylbenzyl bromide

: 167414-69-9
ethyl 3-<1-(methoxycarbonyl)-4-piperidyl>-3-oxopropanoate

: 439944-55-5
ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate

Guidance literature:: With sodium ethanolate; In ethanol; at 80 ℃; for 16h;
DOI:10.1021/jm020027o

Reference yield:

: 197585-43-6
1-methoxycarbonyl-4-piperidinecarboxylic acid chloride

: 439944-55-5
ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / Et₃N; MgCl₂ / ethyl acetate / 20 °C

2: 60 percent / NaOEt / ethanol / 16 h / 80 °C

With sodium ethanolate; triethylamine; magnesium chloride; In ethanol; ethyl acetate;
DOI:10.1021/jm020027o

Reference yield:

: 197585-42-5
1-(methoxycarbonyl)piperidine-4-carboxylic acid

: 439944-55-5
ethyl 3-(1-methoxycarbonyl-4-piperidyl)-3-oxo-2-(4-phenylbenzyl)propionate

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / SOCl₂ / dimethylformamide / 0.33 h / 85 °C

2: 65 percent / Et₃N; MgCl₂ / ethyl acetate / 20 °C

3: 60 percent / NaOEt / ethanol / 16 h / 80 °C

With thionyl chloride; sodium ethanolate; triethylamine; magnesium chloride; In ethanol; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm020027o