N,N-Diethylcyclopent-1-en-1-amine

Base Information

• Chemical Name: N,N-Diethylcyclopent-1-en-1-amine
• CAS No.: 34969-48-7
• Molecular Formula: C9H17N
• Molecular Weight: 139.241
• DSSTox Substance ID: DTXSID60562139
• Nikkaji Number: J594.941F
• Wikidata: Q82446164
• Mol file: 34969-48-7.mol

Synonyms:34969-48-7;N,N-Diethylcyclopent-1-en-1-amine;SCHEMBL516442;Cyclopent-1-enyl-diethyl-amine;DTXSID60562139

Chemical Property of N,N-Diethylcyclopent-1-en-1-amine

Chemical Property:

• Boiling Point: 199.1±10.0 °C(Predicted)
• PSA: 3.24000
• Density: 0.87±0.1 g/cm3(Predicted)
• LogP: 2.39600
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 139.136099547
• Heavy Atom Count: 10
• Complexity: 123

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN(CC)C1=CCCC1

Technology Process of N,N-Diethylcyclopent-1-en-1-amine

There total 1 articles about N,N-Diethylcyclopent-1-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: 56.0%

1-Diaethylamino-1-tributylstannyloxy-cyclopentan → 1-(N,N-diethylamino)cyclopentene (34969-48-7) + (CH3CH2CH2CH2)3SnOC5H7 (17851-95-5) + bis(tri-n-butyltin)oxide (56-35-9)

Guidance literature:

byproducts: H2O, NH(C2H5)2; decompn. at 100°C for 6 h;

DOI:10.1016/S0022-328X(00)81096-7

Reference yield: 50.0%

1-(N,N-diethylamino)cyclopentene (34969-48-7) + O-ethoxycarbonyl-1-phenyl-2-propyn-1-ol → (1S,4R,5R)-4-phenylbicyclo[3.2.1]oct-2-en-8-one

Guidance literature:

With C₃₀H₂₇FeN₂P; copper(II) acetate monohydrate; N-ethyl-N,N-diisopropylamine; In ethanol; at 0 ℃; for 12h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;

DOI:10.1021/ja303129s

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