(2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one

Base Information

• Chemical Name: (2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one
• CAS No.: 699432-88-7
• Molecular Formula: C₂₀H₃₂N₂O₂
• Molecular Weight: 332.486
• Mol file: 699432-88-7.mol

Synonyms:(2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one

Chemical Property of (2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one

There total 5 articles about (2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one 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: 96.0%

acetic acid 2-(3-acetyl-2-tert-butyl-1-methyl-5-oxo-imidazolidin-4-yl)-1-(4-tert-butyl-phenyl)-ethyl ester (699432-83-2) → (2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one (699432-88-7)

Guidance literature:

With potassium carbonate; In methanol; for 1.5h; Heating;

DOI:10.1021/ol049505a

Reference yield:

4-tert-Butylstyrene (1746-23-2,26009-55-2) → (2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one (699432-88-7)

Guidance literature:

Multi-step reaction with 3 steps

1: 91 percent / 1,2-dichloro-ethane / 5 h / Heating

2: 86 percent / Zn / 20 h

3: 96 percent / K₂CO₃ / methanol / 1.5 h / Heating

With potassium carbonate; zinc; In methanol; 1,2-dichloro-ethane;

DOI:10.1021/ol049505a

Reference yield:

(2R)-2-(tert-butyl)-3-methylimidazolidin-4-one (101143-56-0) → (2R,5S,2'S)-2-tert-butyl-5-[2'-(4''-tert-butylphenyl)-2'-hydroxyethyl]-3-methylimidazolidin-4-one (699432-88-7)

Guidance literature:

Multi-step reaction with 4 steps

1: 80 percent / methyltrioxorhenium; urea-hydrogen peroxide / methanol / 24 h / 0 - 20 °C

2: 91 percent / 1,2-dichloro-ethane / 5 h / Heating

3: 86 percent / Zn / 20 h

4: 96 percent / K₂CO₃ / methanol / 1.5 h / Heating

With urea-hydrogen peroxide; methyltrioxorhenium(VII); potassium carbonate; zinc; In methanol; 1,2-dichloro-ethane;

DOI:10.1021/ol049505a

upstream raw materials:

acetic acid 2-(3-acetyl-2-tert-butyl-1-methyl-5-oxo-imidazolidin-4-yl)-1-(4-tert-butyl-phenyl)-ethyl ester

4-tert-Butylstyrene

(2R)-2-(tert-butyl)-3-methylimidazolidin-4-one

(R)-2-tert-butyl-3-methyl-2,3-dihydroimidazol-4-one N-oxide