2-(2-hydroxy-1-phenyl-ethylimino)-4,5-diphenyl-imidazolidine-1-carboxylic acid ethyl ester

Base Information

Chemical Name:2-(2-hydroxy-1-phenyl-ethylimino)-4,5-diphenyl-imidazolidine-1-carboxylic acid ethyl ester
CAS No.:314050-54-9
Molecular Formula:C₂₆H₂₇N₃O₃
Molecular Weight:429.519
Hs Code.:

Synonyms:2-(2-hydroxy-1-phenyl-ethylimino)-4,5-diphenyl-imidazolidine-1-carboxylic acid ethyl ester

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Chemical Property of 2-(2-hydroxy-1-phenyl-ethylimino)-4,5-diphenyl-imidazolidine-1-carboxylic acid ethyl ester

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Technology Process of 2-(2-hydroxy-1-phenyl-ethylimino)-4,5-diphenyl-imidazolidine-1-carboxylic acid ethyl ester

There total 6 articles about 2-(2-hydroxy-1-phenyl-ethylimino)-4,5-diphenyl-imidazolidine-1-carboxylic acid ethyl ester 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: 100.0%

: 314050-52-7
(4S,5S)-2-[(R)-2-(tert-butyldimethylsilyloxy)-1-phenylethylimino]-4,5-diphenyl-1-ethoxycarbonylimidazolidine

: 314050-54-9
(4S,5S)-4,5-diphenyl-1-ethoxycarbonyl-2-[(R)-2-hydroxy-1-phenylethylimino]imidazolidine

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 3h;
DOI:10.1021/jo000746f

Reference yield:

: 314050-49-2
N-[(R)-2-(tert-butyldimethylsilyloxy)-1-phenylethyl]-N'-[(1S,2S)-1,2-diphenyl-2-(ethoxycarbonylamino)ethyl]thiourea

: 314050-54-9
(4S,5S)-4,5-diphenyl-1-ethoxycarbonyl-2-[(R)-2-hydroxy-1-phenylethylimino]imidazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / 2-chloro-1,3-dimethylimidazolinium chloride; Et₃N / acetonitrile / 24 h / Heating

2: 100 percent / tetrabutylammonium fluoride / tetrahydrofuran / 3 h / 20 °C

With tetrabutyl ammonium fluoride; 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine; In tetrahydrofuran; acetonitrile; 1: Cyclization / 2: Elimination;
DOI:10.1021/jo000746f

Reference yield:

: 56613-80-0
D-2-phenylglycinol

: 314050-54-9
(4S,5S)-4,5-diphenyl-1-ethoxycarbonyl-2-[(R)-2-hydroxy-1-phenylethylimino]imidazolidine

Guidance literature:: Multi-step reaction with 6 steps

1: 94 percent / Et₃N; 4-(dimethylamino)pyridine / CH₂Cl₂ / 24 h / 20 °C

2: Et₃N / CH₂Cl₂ / 1 h / 20 °C

3: 2-chloro-1,3-dimethylimidazolinium chloride / CH₂Cl₂ / 1.2 h / 20 °C

4: 100 percent / CH₂Cl₂ / 25 h / Heating

5: 74 percent / 2-chloro-1,3-dimethylimidazolinium chloride; Et₃N / acetonitrile / 24 h / Heating

6: 100 percent / tetrabutylammonium fluoride / tetrahydrofuran / 3 h / 20 °C

With dmap; tetrabutyl ammonium fluoride; 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine; In tetrahydrofuran; dichloromethane; acetonitrile; 1: Substitution / 2: Substitution / 3: dehydrosulfination / 4: Substitution / 5: Cyclization / 6: Elimination;
DOI:10.1021/jo000746f