1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine

Base Information

• Chemical Name: 1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine
• CAS No.: 878551-85-0
• Molecular Formula: C₃₀H₃₃NO₃
• Molecular Weight: 455.597
• Mol file: 878551-85-0.mol

Synonyms:1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine

Chemical Property of 1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine

There total 7 articles about 1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine 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: 71.0%

1-[2-(4-bromophenoxy)ethyl]piperidine (836-58-8) + 2-(4-methoxyphenyl)-5-methoxy-1-indanone (7478-21-9) → 1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine (878551-85-0)

Guidance literature:

1-[2-(4-bromophenoxy)ethyl]piperidine; With iodine; magnesium; In tetrahydrofuran; for 4h; Heating;

2-(4-methoxyphenyl)-5-methoxy-1-indanone; In tetrahydrofuran; for 20h; Heating;

DOI:10.1021/jm050226i

Reference yield:

1-bromomethyl-3-methoxybenzene (874-98-6) → 1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine (878551-85-0)

Guidance literature:

Multi-step reaction with 4 steps

1.1: potassium bis(trimethylsilyl)amide / tetrahydrofuran; toluene / -78 - 0 °C

1.2: 78 percent / tetrahydrofuran; toluene / 0 - 25 °C

2.1: oxalyl chloride / CH₂Cl₂ / 1.5 h / 25 °C

3.1: 1.793 g / AlCl₃ / CH₂Cl₂ / 1.5 h / Heating

4.1: Mg; iodine / tetrahydrofuran / 4 h / Heating

4.2: 71 percent / tetrahydrofuran / 20 h / Heating

With aluminium trichloride; oxalyl dichloride; iodine; potassium hexamethylsilazane; magnesium; In tetrahydrofuran; dichloromethane; toluene;

DOI:10.1021/jm050226i

Reference yield:

3-(3-methoxyphenyl)-2-(4-methoxyphenyl)propanoyl chloride (866021-32-1) → 1-(2-(4-(6-methoxy-2-(4-methoxyphenyl)-1H-inden-3-yl)phenoxy)ethyl)piperidine (878551-85-0)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 1.793 g / AlCl₃ / CH₂Cl₂ / 1.5 h / Heating

2.1: Mg; iodine / tetrahydrofuran / 4 h / Heating

2.2: 71 percent / tetrahydrofuran / 20 h / Heating

With aluminium trichloride; iodine; magnesium; In tetrahydrofuran; dichloromethane;

DOI:10.1021/jm050226i

upstream raw materials:

1-[2-(4-bromophenoxy)ethyl]piperidine

2-(4-methoxyphenyl)-5-methoxy-1-indanone

3-(3-methoxyphenyl)-2-(4-methoxyphenyl)propanoyl chloride

4-Methoxyphenylacetic acid