(2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:(2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester
CAS No.:239802-29-0
Molecular Formula:C₂₃H₂₉NO₄
Molecular Weight:383.488
Hs Code.:

Synonyms:(2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester

Suppliers and Price of (2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester

There total 12 articles about (2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-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: 90.0%

: 239802-28-9
(2S,3S,6S)-3-Benzyloxy-6-methoxycarbonylmethyl-2-methyl-piperidine-1-carboxylic acid benzyl ester

: 239802-29-0
(2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: With lithium triethylborohydride; In tetrahydrofuran;
DOI:10.1021/jo990397t

Reference yield:

: 100-39-0
benzyl bromide

: 239802-29-0
(2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: NaH / dimethylformamide; benzene / 80 °C

2: 96 percent / Lawesson's reagent / tetrahydrofuran / Heating

3: 83 percent / PPh₃, Et₃N / acetonitrile / Heating

4: H₂ / Pd(OH)2 / methanol

5: K₂CO₃ / CH₂Cl₂; H₂O

6: 90 percent / Super-Hydride / tetrahydrofuran

With Lawessons reagent; hydrogen; sodium hydride; lithium triethylborohydride; potassium carbonate; triethylamine; triphenylphosphine; palladium dihydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1021/jo990397t

Reference yield:

: 92912-21-5
ethyl 1-benzyl-3,6-dioxo-2-piperidinecarboxylate

: 239802-29-0
(2S,3S,6S)-3-Benzyloxy-6-(2-hydroxy-ethyl)-2-methyl-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 12 steps

1: 88 percent / baker's yeast / H₂O

2: 98 percent / Huenig base / CHCl₃ / Heating

3: 96 percent / Super-Hydride / tetrahydrofuran / 0 °C

4: 95 percent / n-Bu₃P, pyridine

5: 95 percent / Raney Ni (W-4) / ethanol

6: conc. HCl / methanol

7: NaH / dimethylformamide; benzene / 80 °C

8: 96 percent / Lawesson's reagent / tetrahydrofuran / Heating

9: 83 percent / PPh₃, Et₃N / acetonitrile / Heating

10: H₂ / Pd(OH)2 / methanol

11: K₂CO₃ / CH₂Cl₂; H₂O

12: 90 percent / Super-Hydride / tetrahydrofuran

With Lawessons reagent; pyridine; hydrogenchloride; baker's yeast; tributylphosphine; Raney Ni (W-4); hydrogen; sodium hydride; lithium triethylborohydride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; palladium dihydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1021/jo990397t