(R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Base Information

Chemical Name:(R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
CAS No.:1300040-36-1
Molecular Formula:C₂₂H₁₈F₃NO₅
Molecular Weight:433.384
Hs Code.:

Synonyms:(R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

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Chemical Property of (R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

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Technology Process of (R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

There total 4 articles about (R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate 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: 74.0%

: 1300040-40-7
(R)-4-hydroxy-6-(hydroxy(phenyl)methyl)pyridin-2(1H)-one

: 20445-31-2
R-(+)-α-trifluoromethyl-α-methoxy-phenylacetic acid

: 1300040-36-1
(R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; at 0 - 20 ℃; for 8h; regioselective reaction; Inert atmosphere;
DOI:10.1016/j.ejmech.2011.02.039

Reference yield:

: 1228555-59-6
C₁₉H₁₄ClNO₂

: 1300040-36-1
(R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: water; acetic acid / 12 h / 180 - 190 °C / Sealed vessel

2.1: (+)-B-chlorodiisopinocampheylborane / tetrahydrofuran / 12 h / -40 - -10 °C / Inert atmosphere

2.2: Inert atmosphere; Cooling with ice

3.1: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran; dichloromethane / 8 h / 0 - 20 °C / Inert atmosphere

With dmap; water; acetic acid; dicyclohexyl-carbodiimide; (+)-B-chlorodiisopinocampheylborane; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.ejmech.2011.02.039

Reference yield:

: 1300040-33-8
(6-chloro-4-hydroxypyridin-2-yl)(phenyl)methanone

: 1300040-36-1
(R)-((R)-(4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)(phenyl)methyl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: water; acetic acid / 7 h / 180 - 190 °C / Sealed vessel

2.1: (+)-B-chlorodiisopinocampheylborane / tetrahydrofuran / 12 h / -40 - -10 °C / Inert atmosphere

2.2: Inert atmosphere; Cooling with ice

3.1: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran; dichloromethane / 8 h / 0 - 20 °C / Inert atmosphere

With dmap; water; acetic acid; dicyclohexyl-carbodiimide; (+)-B-chlorodiisopinocampheylborane; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.ejmech.2011.02.039