tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate

Base Information

Chemical Name:tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate
CAS No.:1067884-93-8
Molecular Formula:C₂₃H₃₃NO₃
Molecular Weight:371.52
Hs Code.:

Synonyms:tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate

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Chemical Property of tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate

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Technology Process of tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate

There total 1 articles about tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate 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:

: 1067884-86-9
tert-butyl 3-(1-ethyl-2,4-dioxocyclohex-1-yl)propanoate

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

: 1067884-93-8
tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate

: 1067885-25-9
tert-butyl 3-{(1R)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate

Guidance literature:: With zinc trifluoromethanesulfonate; In acetonitrile; at 60 ℃; for 3h;
DOI:10.1021/jo801316s

Reference yield: 75.0%

: 1067884-93-8
tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate

: 1067884-95-0
(+)-(S)-1-Ethyl-2-oxo-4-methoxy-3-cyclohexene-1-propanoic acid methyl ester

Guidance literature:: tert-butyl 3-{(1S)-1-ethyl-4-[(S)-1-phenylethyl]amino-2-oxocyclohex-3-en-1-yl}propanoate; With chloroformic acid ethyl ester; sodium hydride; In dichloromethane; at 20 ℃; for 22h;

With hydrogenchloride; In methanol; at 60 ℃; for 16h; Further stages.;
DOI:10.1021/jo801316s