(1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic acid methyl ester

Base Information

• Chemical Name: (1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic acid methyl ester
• CAS No.: 476187-19-6
• Molecular Formula: C₁₆H₂₃NO₃
• Molecular Weight: 277.364
• Mol file: 476187-19-6.mol

Synonyms:(1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic acid methyl ester

Chemical Property of (1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic acid methyl ester

There total 6 articles about (1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic 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: 61.0%

(3S)-(8S)-(8aR)-methyl-5-oxo-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-8-carboxylic acid methyl ester (454451-67-3) → (1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic acid methyl ester (476187-19-6)

Guidance literature:

With dimethylsulfide borane complex; In tetrahydrofuran; at 20 ℃; for 24h;

DOI:10.1021/jo025955+ DOI:10.1016/j.tet.2004.04.055

Reference yield:

acetoacetic acid methyl ester (105-45-3) → (1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic acid methyl ester (476187-19-6)

Guidance literature:

Multi-step reaction with 5 steps

1: 100 percent / methanol / 24 h / Heating

2: 100 percent / tetrahydrofuran / 0.25 h / 0 °C

3: 88 percent / HF*pyridine / tetrahydrofuran / 0 - 20 °C

4: 100 percent / LiHMDS / tetrahydrofuran / 2 h / 0 °C

5: 61 percent / BH₃*Me₂S / tetrahydrofuran / 24 h / 20 °C

With dimethylsulfide borane complex; pyridine hydrogenfluoride; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; 4: intramolecular Michael addition;

DOI:10.1016/j.tet.2004.04.055

Reference yield:

(S)-2-(tert-butyldimethylsilyloxy)-1-phenylethylamine (120417-13-2) → (1S)-(2S)-(3S)-1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-piperidine-3-carboxylic acid methyl ester (476187-19-6)

Guidance literature:

Multi-step reaction with 5 steps

1: 100 percent / methanol / 24 h / Heating

2: 100 percent / tetrahydrofuran / 0.25 h / 0 °C

3: 88 percent / HF*pyridine / tetrahydrofuran / 0 - 20 °C

4: 100 percent / LiHMDS / tetrahydrofuran / 2 h / 0 °C

5: 61 percent / BH₃*Me₂S / tetrahydrofuran / 24 h / 20 °C

With dimethylsulfide borane complex; pyridine hydrogenfluoride; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; 4: intramolecular Michael addition;

DOI:10.1016/j.tet.2004.04.055

upstream raw materials:

(3S)-(8S)-(8aR)-methyl-5-oxo-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-8-carboxylic acid methyl ester

(S)-2-(tert-butyldimethylsilyloxy)-1-phenylethylamine

acetoacetic acid methyl ester

1-(2-hydroxy-(1S)-phenyl-ethyl)-2-methyl-6-oxo-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid methyl ester

Downstream raw materials:

(2S,3S)-2-Methyl-piperidine-3-carboxylic acid methyl ester