2--N-<(S)-α-phenylethyl>benzamide

Base Information

Chemical Name:2--N-<(S)-α-phenylethyl>benzamide
CAS No.:223756-05-6
Molecular Formula:C₁₈H₁₉ClN₂O₂
Molecular Weight:330.814
Hs Code.:

2-<N-(chloroacetyl)methylamino>-N-<(S)-α-phenylethyl>benzamide

Synonyms:2--N-<(S)-α-phenylethyl>benzamide

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Chemical Property of 2--N-<(S)-α-phenylethyl>benzamide

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Technology Process of 2--N-<(S)-α-phenylethyl>benzamide

There total 3 articles about 2--N-<(S)-α-phenylethyl>benzamide 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: 88.0%

: 79-04-9
chloroacetyl chloride

: 215929-67-2
2-(methylamino)-N-<(S)-α-phenylethyl>benzamide

: 223756-05-6
2--N-<(S)-α-phenylethyl>benzamide

Guidance literature:: With triethylamine; In dichloromethane; 1) 0 deg C, 1.5 h; 2) rt, 1 h;
DOI:10.1021/jo980777z

Reference yield:

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

: 223756-05-6
2--N-<(S)-α-phenylethyl>benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / ethyl acetate / 35 °C

2: 88 percent / Et₃N / CH₂Cl₂ / 1) 0 deg C, 1.5 h; 2) rt, 1 h

With triethylamine; In dichloromethane; ethyl acetate;
DOI:10.1021/jo980777z

Reference yield:

: 10328-92-4
N-Methylisatoic anhydride

: 223756-05-6
2--N-<(S)-α-phenylethyl>benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / ethyl acetate / 35 °C

2: 88 percent / Et₃N / CH₂Cl₂ / 1) 0 deg C, 1.5 h; 2) rt, 1 h

With triethylamine; In dichloromethane; ethyl acetate;
DOI:10.1021/jo980777z