(2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol

Base Information

Chemical Name:(2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol
CAS No.:1618092-58-2
Molecular Formula:C₁₈H₂₂ClNO₂S
Molecular Weight:351.897
Hs Code.:

Synonyms:(2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol

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Chemical Property of (2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol

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Technology Process of (2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol

There total 6 articles about (2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol 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: 91.0%

: 1618092-57-1
(4R)-4-(2-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}ethyl)-4-methyl-1,3-oxazolidin-2-one

: 1618092-58-2
(2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol

Guidance literature:: With methanol; potassium hydroxide; In tetrahydrofuran; for 12h; Reflux;
DOI:10.1016/j.tet.2014.05.086

Reference yield: 91.0%

: C₁₂H₁₅NO₂

: 1618092-58-2
(2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol

Guidance literature:: With potassium hydroxide; In tetrahydrofuran; methanol; water; for 12h; Reflux;
DOI:10.1016/j.tet.2014.05.086

Reference yield:

: 509089-07-0
2-chloro-4-[(3-methoxyphenyl)sulfanyl]benzaldehyde

: 1618092-58-2
(2R)-2-amino-4-{2-chloro-4-[(3-methoxyphenyl)sulfanyl]phenyl}-2-methyl-butan-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C

1.2: 2 h / -78 - 20 °C

2.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 6 h / 20 °C

3.1: potassium hydroxide; methanol / tetrahydrofuran / 12 h / Reflux

With methanol; n-butyllithium; palladium 10% on activated carbon; hydrogen; potassium hydroxide; In tetrahydrofuran; hexane; ethyl acetate;
DOI:10.1016/j.tet.2014.05.086