(2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on

Base Information

• Chemical Name: (2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on
• CAS No.: 97443-93-1
• Molecular Formula: C₁₈H₂₆N₂O₂
• Molecular Weight: 302.417
• Mol file: 97443-93-1.mol

Synonyms:(2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on

Chemical Property of (2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on

There total 3 articles about (2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on 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: 78.0%

benzoic acid anhydride (93-97-0) + (S)-N-(2',2'-Dimethylpropyliden)valin-(N-methylamid) → (2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on (97443-93-1) + (2S,5S)-1-Benzoyl-2-tert-butyl-5-isopropyl-3-methyl-imidazolidin-4-one

Guidance literature:

at 140 ℃; for 1h;

DOI:10.1002/hlca.19850680117

Reference yield:

L-valine N-methylamide (87105-26-8) → (2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on (97443-93-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 76 percent / pentane / Heating

2: 78 percent / 1 h / 140 °C

In pentane;

DOI:10.1002/hlca.19850680117

Reference yield:

pivalaldehyde (630-19-3) → (2R,5S)-1-Benzoyl-2-(tert-butyl)-5-isopropyl-3-methylimidazolidin-4-on (97443-93-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 76 percent / pentane / Heating

2: 78 percent / 1 h / 140 °C

In pentane;

DOI:10.1002/hlca.19850680117

upstream raw materials:

benzoic acid anhydride

L-valine N-methylamide

pivalaldehyde

Downstream raw materials:

(2R,5S)-1-benzoyl-2-(tert-butyl)-5-isopropyl-3,5-dimethylimidazolidin-4-one

(S)-α-Methylvaline