(S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate

Base Information

Chemical Name:(S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate
CAS No.:1286756-07-7
Molecular Formula:C₁₆H₁₉NO₃
Molecular Weight:273.332
Hs Code.:

Synonyms:(S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-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 (S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate

Chemical Property:

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Technology Process of (S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate

There total 3 articles about (S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-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:

: C₁₆H₁₉N₃O₃

: 1286756-07-7
(S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate

Guidance literature:: With silver benzoate; In dichloromethane; at 20 ℃; Darkness;
DOI:10.1021/ol200358h

Reference yield:

: 1286755-94-9
(S)-1-diazo-3-((1-phenylethyl)amino)propan-2-one

: 1286756-07-7
(S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / 20 °C

2: silver benzoate / dichloromethane / 20 °C / Darkness

With silver benzoate; In ethanol; dichloromethane; 1: aza-Michael addition / 2: Wolff rearrangement;
DOI:10.1021/ol200358h

Reference yield:

: 2627-86-3
(S)-1-phenyl-ethylamine

: 1286756-07-7
(S)-ethyl 4-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 1,2-dichloro-ethane / 3 h / 50 °C

2: ethanol / 20 °C

3: silver benzoate / dichloromethane / 20 °C / Darkness

With silver benzoate; In ethanol; dichloromethane; 1,2-dichloro-ethane; 2: aza-Michael addition / 3: Wolff rearrangement;
DOI:10.1021/ol200358h