2,6-Bis(4-methoxyphenyl)-3-phenyl-4-piperidinone oxime

Base Information

• Chemical Name: 2,6-Bis(4-methoxyphenyl)-3-phenyl-4-piperidinone oxime
• CAS No.: 124069-17-6
• Molecular Formula: C25H26 N2 O3
• Molecular Weight: 402.48554
• Mol file: 124069-17-6.mol

Synonyms:BRN 3632722;124069-17-6;2,6-Bis(4-methoxyphenyl)-3-phenyl-4-piperidinone oxime;4-Piperidinone, 2,6-bis(4-methoxyphenyl)-3-phenyl-, oxime;2,6-Bis(4-methoxyphenyl)-3-phenyl-4-piperidinamine oxime;(NE)-N-[2,6-bis(4-methoxyphenyl)-3-phenylpiperidin-4-ylidene]hydroxylamine;GCLAIBRPWZANLY-SLEBQGDGSA-N;LS-117223

Chemical Property of 2,6-Bis(4-methoxyphenyl)-3-phenyl-4-piperidinone oxime

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Boiling Point: 588.2°Cat760mmHg
• Flash Point: 309.6°C
• PSA: 63.08000
• Density: 1.18g/cm³
• LogP: 5.42230
• XLogP3: 4.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 402.19434270
• Heavy Atom Count: 30
• Complexity: 547

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C2CC(=NO)C(C(N2)C3=CC=C(C=C3)OC)C4=CC=CC=C4
• Isomeric SMILES: COC1=CC=C(C=C1)C2C/C(=N\O)/C(C(N2)C3=CC=C(C=C3)OC)C4=CC=CC=C4

Technology Process of 2,6-Bis(4-methoxyphenyl)-3-phenyl-4-piperidinone oxime

There total 3 articles about 2,6-Bis(4-methoxyphenyl)-3-phenyl-4-piperidinone oxime 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: 100.0%

3-phenyl-2,6-di-(p-methoxyphenyl)-4-oxopiperidine (124069-08-5) → 2,6-Bis-(4-methoxy-phenyl)-3-phenyl-piperidin-4-one oxime (124069-17-6)

Guidance literature:

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

DOI:10.1007/BF00758420

Reference yield:

4-methoxy-benzaldehyde (123-11-5) → 2,6-Bis-(4-methoxy-phenyl)-3-phenyl-piperidin-4-one oxime (124069-17-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 48 percent / ammonium acetate / acetic acid / 15 h / 20 °C

2: 100 percent / hydroxylamine hydrochloride / ethanol / 3 h / 85 °C

With ammonium acetate; hydroxylamine hydrochloride; In ethanol; acetic acid;

DOI:10.1007/BF00758420

Reference yield:

1-phenyl-acetone (103-79-7,136675-26-8) → 2,6-Bis-(4-methoxy-phenyl)-3-phenyl-piperidin-4-one oxime (124069-17-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 48 percent / ammonium acetate / acetic acid / 15 h / 20 °C

2: 100 percent / hydroxylamine hydrochloride / ethanol / 3 h / 85 °C

With ammonium acetate; hydroxylamine hydrochloride; In ethanol; acetic acid;

DOI:10.1007/BF00758420

upstream raw materials:

3-phenyl-2,6-di-(p-methoxyphenyl)-4-oxopiperidine

4-methoxy-benzaldehyde

1-phenyl-acetone

Downstream raw materials:

2,6-Bis-(4-methoxy-phenyl)-3-phenyl-piperidin-4-ylamine