Cyclopentanecarboxylic acid, 2-oxo-1-phenyl-, ethyl ester

Base Information

• Chemical Name: Cyclopentanecarboxylic acid, 2-oxo-1-phenyl-, ethyl ester
• CAS No.: 55285-80-8
• Molecular Formula: C14H16O3
• Molecular Weight: 232.279
• DSSTox Substance ID: DTXSID80444403
• Nikkaji Number: J819.834I

Synonyms:55285-80-8;Cyclopentanecarboxylic acid, 2-oxo-1-phenyl-, ethyl ester;DTXSID80444403;1-Phenyl-2-oxocyclopentanecarboxylic acid ethyl ester

Chemical Property of Cyclopentanecarboxylic acid, 2-oxo-1-phenyl-, ethyl ester

Chemical Property:

• XLogP3: 2.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 232.109944368
• Heavy Atom Count: 17
• Complexity: 305

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)C1(CCCC1=O)C2=CC=CC=C2

Technology Process of Cyclopentanecarboxylic acid, 2-oxo-1-phenyl-, ethyl ester

There total 14 articles about Cyclopentanecarboxylic acid, 2-oxo-1-phenyl-, ethyl ester 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: 91.0%

triphenyl bismuth (2+); dichloride (507233-69-4,594-30-9,28719-54-2) + 2-ethoxycarbonyl-1-cyclopentanone (611-10-9) → ethyl 2-oxo-1-phenylcyclopentane-1-carboxylate (55285-80-8)

Guidance literature:

With N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; In benzene; at 80 ℃; for 2h;

Reference yield: 83.0%

phenyllead(IV) triacetate (3076-54-8) + 2-ethoxycarbonyl-1-cyclopentanone (611-10-9) → ethyl 2-oxo-1-phenylcyclopentane-1-carboxylate (55285-80-8)

Guidance literature:

With pyridine; In chloroform; at 40 ℃; for 1h;

Reference yield: 82.0%

2-ethoxycarbonyl-1-cyclopentanone (611-10-9) + phenyl(2,4,6-trimethoxyphenyl)iodonium(III) triflate → ethyl 2-oxo-1-phenylcyclopentane-1-carboxylate (55285-80-8)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

DOI:10.1021/jo981065b

upstream raw materials:

2-ethoxycarbonyl-1-cyclopentanone

phenyllead(IV) triacetate

benzylphenylmercury

triphenyl bismuth ⁽²⁺⁾; dichloride

Downstream raw materials:

2-Mercapto-1-phenyl-cyclopent-2-enecarboxylic acid ethyl ester

1-Phenyl-2-thioxo-cyclopentanecarboxylic acid ethyl ester

2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester

2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid ethyl ester

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