2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid ethyl ester

Base Information

• Chemical Name: 2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid ethyl ester
• CAS No.: 81829-63-2
• Molecular Formula: C₂₄H₂₃NO₄
• Molecular Weight: 389.451
• Mol file: 81829-63-2.mol

Synonyms:2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid ethyl ester

Chemical Property of 2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid ethyl ester

There total 4 articles about 2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid 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: 80.0%

5-phenyl-cyclohexane-1,3-dione (493-72-1) + ethyl benzylidenecyanoacetate (2025-40-3) → 2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid ethyl ester (81829-63-2)

Guidance literature:

With morpholine; In ethanol; for 24h; Heating;

Reference yield: 73.0%

5-phenyl-cyclohexane-1,3-dione (493-72-1) + ethyl (E)-2-cyano-3-phenyl-2-propenoate (2169-69-9) → 2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid ethyl ester (81829-63-2)

Guidance literature:

With morpholine; In ethanol; Heating;

Reference yield:

benzaldehyde (100-52-7) → 2-Amino-5-oxo-4,7-diphenyl-5,6,7,8-tetrahydro-4H-chromene-3-carboxylic acid ethyl ester (81829-63-2)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium fluoride monohydrate / 2 h / 60 °C

2: ethylene glycol / 4 h / 80 °C

With potassium fluoride monohydrate; In ethylene glycol;

DOI:10.1002/jhet.2183

upstream raw materials:

5-phenyl-cyclohexane-1,3-dione

ethyl (E)-2-cyano-3-phenyl-2-propenoate

ethyl benzylidenecyanoacetate

benzaldehyde