1-phenethyl-piperidine-3-carboxylic acid p-phenetidide

Base Information

Chemical Name:1-phenethyl-piperidine-3-carboxylic acid p-phenetidide
CAS No.:123103-32-2
Molecular Formula:C₂₂H₂₈N₂O₂
Molecular Weight:352.477
Hs Code.:

1-phenethyl-piperidine-3-carboxylic acid <i>p</i>-phenetidide

Synonyms:

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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 1-phenethyl-piperidine-3-carboxylic acid p-phenetidide

Chemical Property:

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Technology Process of 1-phenethyl-piperidine-3-carboxylic acid p-phenetidide

There total 4 articles about 1-phenethyl-piperidine-3-carboxylic acid p-phenetidide 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:

: 122679-31-6
3-(4-ethoxy-phenylcarbamoyl)-1-phenethyl-pyridinium; bromide

: 123103-32-2
1-phenethyl-piperidine-3-carboxylic acid p-phenetidide

Guidance literature:: With water; platinum; Hydrogenation;
DOI:10.1021/ja01512a051

Reference yield:

: 59-67-6
nicotinic acid

: 123103-32-2
1-phenethyl-piperidine-3-carboxylic acid p-phenetidide

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂; chlorocarbonic acid ethyl ester; triethylamine

2: methanol

3: platinum; ethanol / Hydrogenation

With methanol; ethanol; dichloromethane; chloroformic acid ethyl ester; triethylamine; platinum;
DOI:10.1021/ja01512a051

Reference yield:

: 2326-77-4
N-(4-ethoxy-phenyl)-nicotinamide

: 123103-32-2
1-phenethyl-piperidine-3-carboxylic acid p-phenetidide

Guidance literature:: Multi-step reaction with 2 steps

1: methanol

2: platinum; ethanol / Hydrogenation

With methanol; ethanol; platinum;
DOI:10.1021/ja01512a051