(4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-1-ethoxycarbonylimidazolidine

Base Information

Chemical Name:(4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-1-ethoxycarbonylimidazolidine
CAS No.:313696-02-5
Molecular Formula:C₂₈H₃₁N₃O₂
Molecular Weight:441.573
Hs Code.:

Synonyms:(4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-1-ethoxycarbonylimidazolidine

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Chemical Property of (4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-1-ethoxycarbonylimidazolidine

Chemical Property:

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Technology Process of (4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-1-ethoxycarbonylimidazolidine

There total 6 articles about (4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-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: 70.0%

: 313695-91-9
N-[(1S,2S)-1,2-diphenyl-2-ethoxycarbonylaminoethyl]-N'-(2-tert-butylphenyl)thiourea

: 313696-02-5
(4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-1-ethoxycarbonylimidazolidine

Guidance literature:: With 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine; In acetonitrile; Heating;
DOI:10.1021/jo000745n

Reference yield:

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

: 313696-02-5
(4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-1-ethoxycarbonylimidazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / acetonitrile / 15 h / 50 °C

2: 70 percent / 2-chloro-1,3-dimethylimidazolinium chloride; Et₃N / acetonitrile / Heating

With 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine; In acetonitrile; 1: Substitution / 2: Cyclization;
DOI:10.1021/jo000745n

Reference yield:

: 6310-21-0
2-(1,1-dimethylethyl)-benzenamine

: 313696-02-5
(4S,5S)-2-(2-tert-butylphenylimino)-4,5-diphenyl-1-ethoxycarbonylimidazolidine

Guidance literature:: Multi-step reaction with 4 steps

1: CH₂Cl₂ / 1 h / 20 °C

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

3: 98 percent / acetonitrile / 15 h / 50 °C

4: 70 percent / 2-chloro-1,3-dimethylimidazolinium chloride; Et₃N / acetonitrile / Heating

With 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine; In dichloromethane; acetonitrile; 1: Substitution / 2: Elimination / 3: Substitution / 4: Cyclization;
DOI:10.1021/jo000745n