4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid

Base Information

Chemical Name:4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid
CAS No.:1390644-43-5
Molecular Formula:C₂₄H₂₃NO₄
Molecular Weight:389.451
Hs Code.:

Synonyms:4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid

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Chemical Property of 4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid

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Technology Process of 4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid

There total 2 articles about 4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid 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:

: 356782-33-7
(R,S)-4-phenyl-2-chromanone-6-carboxylic acid

: 3886-69-9
(R)-1-phenyl-ethyl-amine

: 1390644-43-5
4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid

Guidance literature:: In acetone; at 25 - 35 ℃; for 2h;

Reference yield:

: 99-96-7
4-hydroxy-benzoic acid

: 1390644-43-5
4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: sulfuric acid; acetic acid / 16 h / 100 °C

2: acetone / 2 h / 25 - 35 °C

With sulfuric acid; acetic acid; In acetone;

Reference yield:

: 1390644-43-5
4-hydroxy-3-((R)-3-oxo-1-phenyl-3-((R)-1-phenylethylamino)propyl)benzoic acid

: 286930-02-7,250214-44-9
fesoterodine

Guidance literature:: Multi-step reaction with 4 steps

1: boron trifluoride diethyl etherate / tetrahydrofuran / 1 h / -20 °C

2: hydrogen / 5%-palladium/activated carbon / methanol / 18 h / 25 - 35 °C / 2942.29 Torr / autoclave

3: potassium carbonate / acetone / 6 h / Reflux

4: sodium hydrogencarbonate / dichloromethane; water / 0.5 h / 0 - 5 °C / Inert atmosphere

With boron trifluoride diethyl etherate; hydrogen; sodium hydrogencarbonate; potassium carbonate; 5%-palladium/activated carbon; In tetrahydrofuran; methanol; dichloromethane; water; acetone;