2,3,6-Triphenylpiperidin-4-one

Base Information

• Chemical Name: 2,3,6-Triphenylpiperidin-4-one
• CAS No.: 124069-05-2
• Molecular Formula: C23H21 N O
• Molecular Weight: 0
• DSSTox Substance ID: DTXSID60924697
• Mol file: 124069-05-2.mol

Synonyms:2,3,6-triphenylpiperidin-4-one;2,3,6-Triphenyl-4-oxopiperidine;124069-05-2;4-Piperidinone, 2,3,6-triphenyl-;2,3,6-Triphenyl4-piperidinamine;2,3,6-triphenyl-4-piperidinone;DTXSID60924697;LS-117285

Chemical Property of 2,3,6-Triphenylpiperidin-4-one

Chemical Property:

• Vapor Pressure: 6.31E-10mmHg at 25°C
• Boiling Point: 494.7°Cat760mmHg
• Flash Point: 163.2°C
• PSA: 29.10000
• Density: 1.123g/cm³
• LogP: 5.14400
• XLogP3: 4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 327.162314293
• Heavy Atom Count: 25
• Complexity: 429

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(NC(C(C1=O)C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of 2,3,6-Triphenylpiperidin-4-one

There total 1 articles about 2,3,6-Triphenylpiperidin-4-one 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: 43.0%

benzaldehyde (100-52-7) + 1-phenyl-acetone (103-79-7,136675-26-8) → 2,3,6-triphenyl-piperidin-4-one (124069-05-2)

Guidance literature:

With ammonium acetate; In acetic acid; at 20 ℃; for 15h;

DOI:10.1007/BF00758420

Reference yield: 75.0%

2,3,6-triphenyl-piperidin-4-one (124069-05-2) → 2,3,6-Triphenyl-piperidin-4-one oxime (124069-15-4)

Guidance literature:

With hydroxylamine hydrochloride; In ethanol; at 85 ℃; for 3h;

DOI:10.1007/BF00758420

Reference yield: 69.0%

semicarbazide hydrochloride (563-41-7) + 2,3,6-triphenyl-piperidin-4-one (124069-05-2) → 2,3,6-triphenyl-4-oxopiperidine semicarbazone (124069-19-8)

Guidance literature:

With sodium acetate; In methanol; for 4h; Heating;

DOI:10.1080/10426509708043502

upstream raw materials:

benzaldehyde

1-phenyl-acetone

Downstream raw materials:

2,3,6-triphenyl-4-oxopiperidine semicarbazone

2,3,6-triphenyl-4-hydroxypiperidine

2,3,6-Triphenyl-piperidin-4-one oxime

1-Acetyl-4-acetoxy-2,3,6-triphenyl-1,2,3,6-tetrahydropyridine