2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol

Base Information

Chemical Name:2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol
CAS No.:167262-80-8
Molecular Formula:C₂₀H₂₁Cl₂NO₃
Molecular Weight:394.298
Hs Code.:

Synonyms:2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol

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Chemical Property of 2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol

Chemical Property:

Purity/Quality:

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Technology Process of 2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol

There total 4 articles about 2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol 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:

: 1711-05-3
m-anisoyl chloride

: 52423-89-9
3-(3,4-dichloro-phenyl)-3-(2-hydroxy-ethyl)-pyrrolidine

: 167262-80-8
2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol

Guidance literature:: DOI:10.1016/0960-894X(96)00148-5

Reference yield:

: 40878-10-2
3-cyano-3-(3,4-dichloro-phenyl)-pentanedioic acid diethyl ester

: 167262-80-8
2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / H₂, NH₄OH / Raney Ni / ethanol

2: 71 percent / AlH₃ / tetrahydrofuran / 50 °C

With aluminium hydride; ammonium hydroxide; hydrogen; nickel; In tetrahydrofuran; ethanol;
DOI:10.1016/0960-894X(96)00148-5

Reference yield:

: 3218-49-3
3,4-dichloro-benzeneacetonitrile

: 167262-80-8
2-[3-(3,4-dichloro-phenyl)-1-(3-methoxy-benzoyl)-pyrrolidin-3-yl]-ethanol

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / sodium bis(trimethylsilylamide) / tetrahydrofuran

2: 81 percent / H₂, NH₄OH / Raney Ni / ethanol

3: 71 percent / AlH₃ / tetrahydrofuran / 50 °C

With aluminium hydride; ammonium hydroxide; hydrogen; sodium hexamethyldisilazane; nickel; In tetrahydrofuran; ethanol;
DOI:10.1016/0960-894X(96)00148-5