(S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl ester

Base Information

Chemical Name:(S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl ester
CAS No.:1373416-73-9
Molecular Formula:C₂₀H₂₄O₄
Molecular Weight:328.408
Hs Code.:

Synonyms:(S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl ester

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Chemical Property of (S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl ester

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Technology Process of (S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl ester

There total 4 articles about (S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl 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: 86.0%

: 582-17-2
2,7-Dihydroxynaphthalene

: C₁₁H₁₇F₃O₅S

: 1373416-73-9
(S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl ester

Guidance literature:: With potassium carbonate; In acetonitrile; at 20 ℃; for 1.5h; Inert atmosphere;
DOI:10.3998/ark.5550190.0013.311

Reference yield:

: methyl 2-hydroxy-3-phenylpropionate

: 1373416-73-9
(S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen; Rh/Al₂O₃ / tetrahydrofuran; water

2: 2,6-dimethylpyridine / dichloromethane

3: potassium carbonate / acetonitrile / 1.5 h / 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; Rh/Al₂O₃; hydrogen; potassium carbonate; In tetrahydrofuran; dichloromethane; water; acetonitrile;
DOI:10.3998/ark.5550190.0013.311

Reference yield:

: C₁₀H₁₈O₃

: 1373416-73-9
(S)-3-cyclohexyl-2-(7-hydroxynaphthalen-2-yloxy)propionic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 2,6-dimethylpyridine / dichloromethane

2: potassium carbonate / acetonitrile / 1.5 h / 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; potassium carbonate; In dichloromethane; acetonitrile;
DOI:10.3998/ark.5550190.0013.311