(R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl ester

Base Information

Chemical Name:(R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl ester
CAS No.:1456722-42-1
Molecular Formula:C₂₃H₂₉NO₅
Molecular Weight:399.487
Hs Code.:

Synonyms:(R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl ester

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Chemical Property of (R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl ester

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Technology Process of (R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl ester

There total 3 articles about (R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl 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:

: C₂₃H₂₇NO₅

: 1456722-42-1
(R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl ester

Guidance literature:: With diphenyl sulfide; palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 17h; under 760.051 Torr;
DOI:10.1016/j.tet.2013.08.042

Reference yield:

: 117833-92-8
(4S)-3-benzyloxycarbonyl-2,2-dimethyloxazolidine-4-carbaldehyde

: 1456722-42-1
(R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran / 0.58 h / -20 °C / Inert atmosphere

1.2: 1.75 h / -70 - -15 °C / Inert atmosphere

2.1: diphenyl sulfide; hydrogen; palladium 10% on activated carbon / methanol / 17 h / 20 °C / 760.05 Torr

With n-butyllithium; diphenyl sulfide; palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol;
DOI:10.1016/j.tet.2013.08.042

Reference yield:

: (3,4-dimethoxy-benzyl)-triphenyl-phosphonium bromide

: 1456722-42-1
(R)-4-[2-(3,4-dimethoxyphenyl)-ethyl]-2,2-di-methyl-oxazolidine-3 carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran / 0.58 h / -20 °C / Inert atmosphere

1.2: 1.75 h / -70 - -15 °C / Inert atmosphere

2.1: diphenyl sulfide; hydrogen; palladium 10% on activated carbon / methanol / 17 h / 20 °C / 760.05 Torr

With n-butyllithium; diphenyl sulfide; palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol;
DOI:10.1016/j.tet.2013.08.042