5(2H)-Isoxazolone, 3-hydroxy-4-phenyl-2-[phenyl[(phenylmethyl)amino]methyl]-

Base Information

• Chemical Name: 5(2H)-Isoxazolone, 3-hydroxy-4-phenyl-2-[phenyl[(phenylmethyl)amino]methyl]-
• CAS No.: 866097-25-8
• Molecular Formula: C₂₃H₂₀N₂O₃
• Molecular Weight: 372.423
• Mol file: 866097-25-8.mol

Synonyms:5(2H)-Isoxazolone, 3-hydroxy-4-phenyl-2-[phenyl[(phenylmethyl)amino]methyl]-

Chemical Property of 5(2H)-Isoxazolone, 3-hydroxy-4-phenyl-2-[phenyl[(phenylmethyl)amino]methyl]-

Chemical Property:

• PSA: 67.40000
• LogP: 4.54150

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5(2H)-Isoxazolone, 3-hydroxy-4-phenyl-2-[phenyl[(phenylmethyl)amino]methyl]-

There total 3 articles about 5(2H)-Isoxazolone, 3-hydroxy-4-phenyl-2-[phenyl[(phenylmethyl)amino]methyl]- 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: 85.0%

5-oxo-4-phenyl-2-[1-phenylmethylidene]-isoxazol-2-ium-3(5H)-olate (37118-32-4) + benzylamine (100-46-9) → 2-[(benzylamino)(phenyl)methyl]-3-hydroxy-4-phenyl-5(2H)-isoxazolone (866097-25-8)

Guidance literature:

In chloroform; at 20 ℃; for 0.333333h;

DOI:10.1515/HC.2005.11.1.49

Reference yield:

(chlorocarbonyl)phenyl ketene (17118-70-6) → 2-[(benzylamino)(phenyl)methyl]-3-hydroxy-4-phenyl-5(2H)-isoxazolone (866097-25-8)

Guidance literature:

Multi-step reaction with 2 steps

1: diethyl ether / 0 °C

2: 85 percent / CHCl₃ / 0.33 h / 20 °C

In diethyl ether; chloroform;

DOI:10.1515/HC.2005.11.1.49

Reference yield:

Benzaldoxime (932-90-1) → 2-[(benzylamino)(phenyl)methyl]-3-hydroxy-4-phenyl-5(2H)-isoxazolone (866097-25-8)

Guidance literature:

Multi-step reaction with 2 steps

1: diethyl ether / 0 °C

2: 85 percent / CHCl₃ / 0.33 h / 20 °C

In diethyl ether; chloroform;

DOI:10.1515/HC.2005.11.1.49

upstream raw materials:

5-oxo-4-phenyl-2-[1-phenylmethylidene]-isoxazol-2-ium-3(5H)-olate

benzylamine

(chlorocarbonyl)phenyl ketene

Benzaldoxime