1-Pyrrolidineacetamide, N-(phenylmethyl)-

Base Information

• Chemical Name: 1-Pyrrolidineacetamide, N-(phenylmethyl)-
• CAS No.: 42175-93-9
• Molecular Formula: C₁₃H₁₈N₂O
• Molecular Weight: 218.299
• DSSTox Substance ID: DTXSID40194997
• Nikkaji Number: J1.563.412J
• Wikidata: Q83067875
• ChEMBL ID: CHEMBL56715
• Mol file: 42175-93-9.mol

Synonyms:BRN 6058168;1-Pyrrolidineacetamide, N-(phenylmethyl)-;N-benzyl-2-(pyrrolidin-1-yl)acetamide;N-(Phenylmethyl)-1-pyrrolidineacetamide;42175-93-9;CHEMBL56715;N-Benzyl-1-pyrrolidineacetamide;DTXSID40194997;STL072162;AKOS002248596;NCGC00245683-01;LS-137093;Z46169163

Chemical Property of 1-Pyrrolidineacetamide, N-(phenylmethyl)-

Chemical Property:

• Vapor Pressure: 6.9E-07mmHg at 25°C
• Boiling Point: 408.6°Cat760mmHg
• Flash Point: 200.9°C
• Density: 1.088g/cm³
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 218.141913202
• Heavy Atom Count: 16
• Complexity: 218

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN(C1)CC(=O)NCC2=CC=CC=C2

Technology Process of 1-Pyrrolidineacetamide, N-(phenylmethyl)-

There total 2 articles about 1-Pyrrolidineacetamide, N-(phenylmethyl)- 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: 21.0%

1-carboxymethylpyrrolidone-2 N-benzylamide (105479-05-8) → 1-(benzylaminoethyl)-2-hydroxypyrrolidine (105504-31-2) + 1-pyrrolidine-N-benzylacetamide (42175-93-9)

Guidance literature:

With sodium tetrahydroborate; acetic acid; In 1,4-dioxane; for 2h; Yields of byproduct given; Heating;

Reference yield:

2-(oxo-pyrrolidin-1-yl)-acetic acid ethyl ester (61516-73-2) → 1-pyrrolidine-N-benzylacetamide (42175-93-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 65 percent / 6 h / Heating

2: sodium borohydride, acetic acid / dioxane / 2 h / Heating

With sodium tetrahydroborate; acetic acid; In 1,4-dioxane;

upstream raw materials:

1-carboxymethylpyrrolidone-2 N-benzylamide

2-(oxo-pyrrolidin-1-yl)-acetic acid ethyl ester