(4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine

Base Information

Chemical Name:(4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine
CAS No.:894809-33-7
Molecular Formula:C₃₂H₃₁N₃O₃
Molecular Weight:505.616
Hs Code.:

Synonyms:(4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine

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Chemical Property of (4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine

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Technology Process of (4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine

There total 6 articles about (4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine 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: 71.0%

: 894809-32-6
(4S,5S)-2-[(E)-(1S,2R)-(2-t-butyldimethylsilyloxy-1,2-diphenylethyl)]imino-4,5-diphenyl-1-ethoxycarbonylimidazolidine

: 894809-33-7
(4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 24h;
DOI:10.1002/adsc.200505161

Reference yield:

: 203922-97-8
(1S,2S)-2-amino-1,2-diphenyl-1-ethoxycarbonylaminoethane

: 894809-33-7
(4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / CH₂Cl₂ / 65 h / 20 °C

2: 92 percent / Et₃N; 2-chloro-1,3-dimethylimidazolium chloride / acetonitrile / 17 h / Heating

3: 71 percent / tetrabutylammonium fluoride / tetrahydrofuran / 24 h / 20 °C

With 2-chloro-1,3-dimethyl imidazolium chloride; tetrabutyl ammonium fluoride; triethylamine; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1002/adsc.200505161

Reference yield:

: 894809-30-4
(1R,2S)-1-t-butyldimethylsilyloxy-1,2-diphenyl-2-isothiocyanatoethane

: 894809-33-7
(4S,5S)-4,5-diphenyl-2-[(E)-(1S,2R)-(1,2-diphenyl-2-hydroxyethyl)]imino-1-ethoxycarbonylimidazolidine

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / CH₂Cl₂ / 65 h / 20 °C

2: 92 percent / Et₃N; 2-chloro-1,3-dimethylimidazolium chloride / acetonitrile / 17 h / Heating

3: 71 percent / tetrabutylammonium fluoride / tetrahydrofuran / 24 h / 20 °C

With 2-chloro-1,3-dimethyl imidazolium chloride; tetrabutyl ammonium fluoride; triethylamine; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1002/adsc.200505161