(2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine

Base Information

• Chemical Name: (2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine
• CAS No.: 221662-29-9
• Molecular Formula: C₂₂H₂₇NO
• Molecular Weight: 321.462
• Mol file: 221662-29-9.mol

Synonyms:(2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine

Chemical Property of (2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine

There total 5 articles about (2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine 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: 79.0%

N-benzyl(but-3-en-2-yl)amine (37857-30-0) + {[(2Z)-4-Chloro-2-methylbut-2-enyl]oxy}benzene (221662-33-5) → (2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine (221662-29-9)

Guidance literature:

With potassium carbonate; sodium iodide; In acetonitrile; Heating;

DOI:10.1039/b005853j

Reference yield:

3-phenoxy-2-propanone (621-87-4) → (2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine (221662-29-9)

Guidance literature:

Multi-step reaction with 4 steps

1.1: NaH / tetrahydrofuran / 0.5 h

1.2: 32 percent / tetrahydrofuran / 0.5 h / -15 °C

2.1: DIBAL / toluene / 0.5 h / -78 °C

3.1: 372 mg / TsCl; DMAP / CH₂Cl₂

4.1: 79 percent / K₂CO₃; NaI / acetonitrile / Heating

With dmap; sodium hydride; diisobutylaluminium hydride; potassium carbonate; p-toluenesulfonyl chloride; sodium iodide; In tetrahydrofuran; dichloromethane; toluene; acetonitrile; 1.1: Metallation / 1.2: Condensation / 2.1: Reduction / 3.1: Substitution / 4.1: Alkylation;

DOI:10.1039/b005853j

Reference yield:

benzylamine (100-46-9) → (2Z)-N-Benzyl-3-methyl-N-(1-methylprop-2-enyl)-4-phenoxybut-2-en-1-amine (221662-29-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 14 percent / K₂CO₃ / acetonitrile / Heating

2: 79 percent / K₂CO₃; NaI / acetonitrile / Heating

With potassium carbonate; sodium iodide; In acetonitrile; 1: Alkylation / 2: Alkylation;

DOI:10.1039/b005853j

upstream raw materials:

N-benzyl(but-3-en-2-yl)amine

{[(2Z)-4-Chloro-2-methylbut-2-enyl]oxy}benzene

3-phenoxy-2-propanone

benzylamine