(2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-4-one

Base Information

• Chemical Name: (2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-4-one
• CAS No.: 111610-38-9
• Molecular Formula: C₂₃H₃₄N₂O₃
• Molecular Weight: 386.535
• Mol file: 111610-38-9.mol

Synonyms:(2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-4-one

Chemical Property of (2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-4-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-4-one

There total 5 articles about (2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-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: 84.0%

dimethyl sulfate (77-78-1) + (2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-3-methylimidazolidin-4-one (111610-37-8) → (2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-4-one (111610-38-9)

Guidance literature:

With sodium hydroxide; In acetone; at 50 ℃; for 12h;

DOI:10.1002/hlca.19870700129

Reference yield:

(-)-(2R)-2-methyl-4-hexenal (104372-54-5,519002-37-0) → (2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-4-one (111610-38-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 82 percent / (i-Pr)2NH, BuLi / tetrahydrofuran; hexane / 1.) -75 degC, 20 min; 2.) -100 degC, 50 min; 3.) 30 min, r.t.

2: 84 percent / 40 percent aq. NaOH / acetone / 12 h / 50 °C

With sodium hydroxide; n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; acetone;

DOI:10.1002/hlca.19870700129

Reference yield:

benzoyl chloride (98-88-4) → (2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-1,3-dimethylimidazolidin-4-one (111610-38-9)

Guidance literature:

Multi-step reaction with 3 steps

2: 82 percent / (i-Pr)2NH, BuLi / tetrahydrofuran; hexane / 1.) -75 degC, 20 min; 2.) -100 degC, 50 min; 3.) 30 min, r.t.

3: 84 percent / 40 percent aq. NaOH / acetone / 12 h / 50 °C

With sodium hydroxide; n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; acetone;

DOI:10.1002/hlca.19870700129

upstream raw materials:

dimethyl sulfate

(2R,5S,1'R,2'R)-5-((E)-1'-benzoyloxy-2'-methyl-4'-hexenyl)-2-(tert-butyl)-3-methylimidazolidin-4-one

(-)-(2R)-2-methyl-4-hexenal

benzoyl chloride

Downstream raw materials:

(1R,2R,2'S,4E)-1-(N₁,N₂-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate