(1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-amine

Base Information

Chemical Name:(1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-amine
CAS No.:1393836-86-6
Molecular Formula:C₂₁H₂₆N₂
Molecular Weight:306.451
Hs Code.:

Synonyms:

Suppliers and Price of (1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-amine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-amine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-amine

There total 5 articles about (1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-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:

: trifluoroacetate of 5-methylproline methyl ester

: 1393836-86-6
(1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetonitrile / 0.25 h / 0 °C

1.2: 16 h / Reflux

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C / Cooling with ice

3.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 °C

4.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 16 h / 0 - 20 °C

With lithium aluminium tetrahydride; oxalyl dichloride; sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; acetonitrile;

Reference yield:

: 15761-39-4,59433-50-0
N-tert-butoxycarbonyl-proline

: 1393836-86-6
(1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-amine

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 24 h / 0 - 20 °C

2.1: dichloromethane / 4 h / 20 °C / Cooling with ice

3.1: potassium carbonate / acetonitrile / 0.25 h / 0 °C

3.2: 16 h / Reflux

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C / Cooling with ice

5.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 °C

6.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 16 h / 0 - 20 °C

With lithium aluminium tetrahydride; oxalyl dichloride; sodium tris(acetoxy)borohydride; sodium hydride; potassium carbonate; acetic acid; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 145681-01-2
(+/-)-N-tert-butoxycarbonylproline methyl ester

: 1393836-86-6
(1-benzylpyrrolidin-2-ylmethyl)indan-2-yl-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: dichloromethane / 4 h / 20 °C / Cooling with ice

2.1: potassium carbonate / acetonitrile / 0.25 h / 0 °C

2.2: 16 h / Reflux

3.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C / Cooling with ice

4.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 °C

5.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 16 h / 0 - 20 °C

With lithium aluminium tetrahydride; oxalyl dichloride; sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; acetonitrile;