(R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl ester

Base Information

Chemical Name:(R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl ester
CAS No.:630054-42-1
Molecular Formula:C₁₉H₂₇NO₄
Molecular Weight:333.428
Hs Code.:

Synonyms:(R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl ester

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Chemical Property of (R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl ester

Chemical Property:

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Technology Process of (R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl ester

There total 9 articles about (R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl 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:

: 100-39-0
benzyl bromide

: 630054-42-1
(R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / KH / 0.5 h / Heating

2: H₂ / Pd/C / ethanol / 20 °C

3: Et₃N / CH₂Cl₂ / 0 °C

With hydrogen; potassium hydride; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1016/j.tetlet.2003.08.113

Reference yield:

: 136179-92-5
Ethyl (2E)-7-Benzyloxy-2-methylheptenoate

: 630054-42-1
(R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 96 percent / AD-mix-α; MsNH2 / 2-methyl-propan-2-ol; H2O / 0 °C

2: pyridine / CH₂Cl₂ / 0 °C

3: K₂CO₃ / ethanol / 20 °C

4: H₂ / Pd/C / ethanol

5: Et₃N / CH₂Cl₂

6: 97 percent / acetonitrile / 48 h / Heating

7: 95 percent / KH / 0.5 h / Heating

8: H₂ / Pd/C / ethanol / 20 °C

9: Et₃N / CH₂Cl₂ / 0 °C

With pyridine; AD-mix-α; methanesulfonamide; hydrogen; potassium hydride; potassium carbonate; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; water; acetonitrile; tert-butyl alcohol; 1: Sharpless reaction;
DOI:10.1016/j.tetlet.2003.08.113

Reference yield:

: (2R,3R)-3-(4-Hydroxy-butyl)-2-methyl-oxirane-2-carboxylic acid ethyl ester

: 630054-42-1
(R)-2-((S)-1-Acetyl-piperidin-2-yl)-2-benzyloxy-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: Et₃N / CH₂Cl₂

2: 97 percent / acetonitrile / 48 h / Heating

3: 95 percent / KH / 0.5 h / Heating

4: H₂ / Pd/C / ethanol / 20 °C

5: Et₃N / CH₂Cl₂ / 0 °C

With hydrogen; potassium hydride; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; acetonitrile;
DOI:10.1016/j.tetlet.2003.08.113