(R)-5--3-(4-chlorophenyl)pentanoic acid

Base Information

Chemical Name:(R)-5--3-(4-chlorophenyl)pentanoic acid
CAS No.:229182-32-5
Molecular Formula:C₁₆H₂₂ClNO₄
Molecular Weight:327.808
Hs Code.:

(R)-5-<N-(tert-butyloxycarbonyl)amino>-3-(4-chlorophenyl)pentanoic acid

Synonyms:(R)-5--3-(4-chlorophenyl)pentanoic acid

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Chemical Property of (R)-5--3-(4-chlorophenyl)pentanoic acid

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Technology Process of (R)-5--3-(4-chlorophenyl)pentanoic acid

There total 4 articles about (R)-5--3-(4-chlorophenyl)pentanoic 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: 97.0%

: 229182-29-0
(R)-1-(tert-butyloxycarbonyl)-4-(4-chlorophenyl)-2-piperidinone

: 229182-32-5
(R)-5--3-(4-chlorophenyl)pentanoic acid

Guidance literature:: (R)-1-(tert-butyloxycarbonyl)-4-(4-chlorophenyl)-2-piperidinone; With sodium hydroxide; In methanol; water; at 20 ℃; for 0.5h;

With hydrogenchloride; In methanol; water; pH=1;
DOI:10.1016/j.tet.2012.09.001

Reference yield:

: (4R,5R)-4-(4-Chloro-phenyl)-5-hydroxy-2-oxo-piperidine-1-carboxylic acid tert-butyl ester

: 229182-32-5
(R)-5--3-(4-chlorophenyl)pentanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / DMAP / CH₂Cl₂ / 18 h / 25 °C

2: 94 percent / SnBu₃H, di-tert-butyl peroxyoxalate / acetone / 18 h / 25 °C

3: 64 percent / aq. LiOH / tetrahydrofuran / 2 h

With dmap; lithium hydroxide; di-tert-butyl diperoxyoxalate; tri-n-butyl-tin hydride; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1021/jm990076+

Reference yield:

: 229182-28-9
(4R,5R)-1-(tert-butyloxycarbonyl)-4-(4-chlorophenyl)-5--2-piperidone

: 229182-32-5
(R)-5--3-(4-chlorophenyl)pentanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / SnBu₃H, di-tert-butyl peroxyoxalate / acetone / 18 h / 25 °C

2: 64 percent / aq. LiOH / tetrahydrofuran / 2 h

With lithium hydroxide; di-tert-butyl diperoxyoxalate; tri-n-butyl-tin hydride; In tetrahydrofuran; acetone;
DOI:10.1021/jm990076+