Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride

Base Information

Chemical Name:Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride
CAS No.:83750-18-9
Molecular Formula:C₁₄H₁₆ClNO₃*ClH
Molecular Weight:318.2
Hs Code.:

Synonyms:Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride

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Chemical Property of Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride

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Technology Process of Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride

There total 3 articles about Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride 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: 95.0%

: 83750-12-3
(E)-3-(4-Chloro-phenyl)-1-(2,5-dimethyl-4,5-dihydro-oxazol-5-yl)-propenone

: 83750-18-9
Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride

Guidance literature:: With hydrogenchloride; at 20 ℃; for 24h;
DOI:10.1007/BF00506575

Reference yield:

: 104-88-1
4-chlorobenzaldehyde

: 83750-18-9
Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 15percent KOH / methanol / 4 h / 20 °C

2: 95 percent / conc. HCl / 24 h / 20 °C

With hydrogenchloride; potassium hydroxide; In methanol;
DOI:10.1007/BF00506575

Reference yield:

: 77219-13-7
1-(2,5-Dimethyl-4,5-dihydro-oxazol-5-yl)-ethanone

: 83750-18-9
Acetic acid (E)-1-aminomethyl-4-(4-chloro-phenyl)-1-methyl-2-oxo-but-3-enyl ester; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 15percent KOH / methanol / 4 h / 20 °C

2: 95 percent / conc. HCl / 24 h / 20 °C

With hydrogenchloride; potassium hydroxide; In methanol;
DOI:10.1007/BF00506575