4-(4-Oxo-1-piperidinyl)benzaldehyde

Base Information

Chemical Name:4-(4-Oxo-1-piperidinyl)benzaldehyde
CAS No.:79421-47-9
Molecular Formula:C₁₂H₁₃NO₂
Molecular Weight:203.241
Hs Code.:
DSSTox Substance ID:DTXSID901293750

Synonyms:4-(4-Oxo-1-piperidinyl)benzaldehyde;79421-47-9;SCHEMBL13348975;DTXSID901293750

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

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Chemical Property of 4-(4-Oxo-1-piperidinyl)benzaldehyde

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:203.094628657
Heavy Atom Count:15
Complexity:234

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN(CCC1=O)C2=CC=C(C=C2)C=O

Technology Process of 4-(4-Oxo-1-piperidinyl)benzaldehyde

There total 5 articles about 4-(4-Oxo-1-piperidinyl)benzaldehyde 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: 61.0%

: 79421-44-6
4-(4-hydroxy-piperidin-1-yl)-benzaldehyde

: 79421-47-9
4-(4-Oxo-piperidin-1-yl)-benzaldehyde

Guidance literature:: With pyridine; dimethyl sulfoxide; dicyclohexyl-carbodiimide; trifluoroacetic acid; In benzene; ice-water bath temp. - room temp., overnight;
DOI:10.1055/s-1981-29539

Reference yield: 53.0%

: 79421-40-2
4-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)benzaldehyde

: 79421-47-9
4-(4-Oxo-piperidin-1-yl)-benzaldehyde

Guidance literature:: With sulfuric acid; In tetrahydrofuran; for 96h; Ambient temperature;
DOI:10.1055/s-1981-29539

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 79421-47-9
4-(4-Oxo-piperidin-1-yl)-benzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / K₂CO₃ / acetonitrile / 96 h / Heating

2: 61 percent / N,N-Dicyclohexylcarbodiimide,DMSO, pyridine, trifluoroacetic acid / benzene / ice-water bath temp. - room temp., overnight

With pyridine; potassium carbonate; dimethyl sulfoxide; dicyclohexyl-carbodiimide; trifluoroacetic acid; In acetonitrile; benzene;
DOI:10.1055/s-1981-29539