(-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal

Base Information

• Chemical Name: (-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal
• CAS No.: 396714-65-1
• Molecular Formula: C₂₇H₂₈O₄
• Molecular Weight: 416.517
• Mol file: 396714-65-1.mol

Synonyms:(-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal

Chemical Property of (-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal

There total 2 articles about (-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal 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: 68.0%

(1S,2R)-1,2-diphenylethane-1,2-diol (579-43-1) + (-)-(2R)-2-methyl-2-[4-(methoxy)phenyl]pentane-1,5-dial (395656-58-3) → (-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal (396714-65-1)

Guidance literature:

With pyridinium p-toluenesulfonate; In toluene; at 70 ℃; for 9h;

DOI:10.1021/jo0104328

Reference yield:

(R)-2-(4-methoxyphenyl)-2-methylpentane-1,5-diol → (-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal (396714-65-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 88.4 mg / PhI(OAc)2 / CH₂Cl₂ / 4 h / 0 °C

2: 68 percent / pyridinium p-toluenesulfonate / toluene / 9 h / 70 °C

With [bis(acetoxy)iodo]benzene; pyridinium p-toluenesulfonate; In dichloromethane; toluene;

DOI:10.1021/jo0104328

Reference yield: 88.0%

methyl-triphenylphosphonium iodide (2065-66-9) + (-)-(2R)-4-(4,5-diphenyl-1,3-dioxolan-2-yl)-2-methyl-2-[4-(methoxy)phenyl]butanal (396714-65-1) → (+)-(3S)-3-methyl-3-[4-(methoxy)phenyl]pent-4-enyl-4,5-diphenyl-1,3-dioxolane (396714-66-2)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; hexane; at 0 ℃; for 1.5h;

DOI:10.1021/jo0104328

upstream raw materials:

(1S,2R)-1,2-diphenylethane-1,2-diol

(-)-(2R)-2-methyl-2-[4-(methoxy)phenyl]pentane-1,5-dial

Downstream raw materials:

(+)-(3S)-3-methyl-3-[4-(methoxy)phenyl]pent-4-enyl-4,5-diphenyl-1,3-dioxolane

(S)-4-(3,7-dimethylocta-1,6-dien-3-yl)phenol

(+)-(4S)-4-methyl-4-[4-(methoxy)phenyl]hex-5-enal

(S)-1-(3,7-dimethylocta-1,6-dien-3-yl)-4-methoxybenzene