1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide

Base Information

Chemical Name:1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide
CAS No.:1393836-35-5
Molecular Formula:C₂₃H₃₁N₂*I
Molecular Weight:462.417
Hs Code.:

Synonyms:1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide

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Chemical Property of 1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide

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Technology Process of 1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide

There total 4 articles about 1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide 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: 41.8%

: 1393836-82-2
indan-2-yl-[2-(1-methylpyrrolidin-2-yl)ethyl]phenylamine

: 74-88-4
methyl iodide

: 1393836-35-5
1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide

Guidance literature:: In Dichlorofluoromethane; at 20 ℃; for 16h;

Reference yield:

: 62-53-3
aniline

: 1393836-35-5
1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 16 h / 20 °C / Cooling with ice

2.1: sodium amide / toluene / 3 h / 0 - 20 °C

2.2: 16 h / Reflux

3.1: Dichlorofluoromethane / 16 h / 20 °C

With sodium tris(acetoxy)borohydride; sodium amide; acetic acid; In dichloromethane; Dichlorofluoromethane; toluene;

Reference yield:

: 615-13-4
2-indanone

: 1393836-35-5
1,1-dimethyl-2-[2-((indan-2-yl)(phenyl)amino)ethyl]pyrrolidinium iodide

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 16 h / 20 °C / Cooling with ice

2.1: sodium amide / toluene / 3 h / 0 - 20 °C

2.2: 16 h / Reflux

3.1: Dichlorofluoromethane / 16 h / 20 °C

With sodium tris(acetoxy)borohydride; sodium amide; acetic acid; In dichloromethane; Dichlorofluoromethane; toluene;