(2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:(2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-1-carboxylic acid benzyl ester
CAS No.:211614-51-6
Molecular Formula:C₁₉H₂₁NO₃
Molecular Weight:311.381
Hs Code.:

Synonyms:(2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-1-carboxylic acid benzyl ester

Suppliers and Price of (2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-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,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-1-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-1-carboxylic acid benzyl ester

There total 8 articles about (2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-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:

: 211614-47-0
(S)-4-((E)-(S)-3-Methoxymethoxy-3-phenyl-propenyl)-oxazolidin-2-one

: 211614-51-6
(2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / H₂ / PtO₂ / ethyl acetate / 5 h / 23 °C / 760 Torr

2: 92 percent / conc. HCl / methanol / 30 h / 40 °C

3: 60 percent / Et₃N, MsCl / tetrahydrofuran / 48 h / 23 °C

4: 1.) n-BuLi / 1.) THF, hexane, 0 deg C, 30 min, 2.) THF, reflux, 15 h

With hydrogenchloride; n-butyllithium; hydrogen; methanesulfonyl chloride; triethylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1021/jo980396l

Reference yield:

: 211614-44-7
(1R,2R)-5-(tert-butyldiphenylsilyloxy)-1-methoxymethoxy-1-phenyl-pent-3-yn-2-ol

: 211614-51-6
(2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 72 percent / bis(methoxyethoxy)aluminum hydride / diethyl ether; toluene / 5 h / -25 °C

2: 1.) NaH / 1.) Et₂O, -5 deg C to 23 deg C, 2.) xylene, reflux, 6 h

3: 80 percent / n-Bu₄NF / tetrahydrofuran / 12 h

4: 97 percent / H₂ / PtO₂ / ethyl acetate / 5 h / 23 °C / 760 Torr

5: 92 percent / conc. HCl / methanol / 30 h / 40 °C

6: 60 percent / Et₃N, MsCl / tetrahydrofuran / 48 h / 23 °C

7: 1.) n-BuLi / 1.) THF, hexane, 0 deg C, 30 min, 2.) THF, reflux, 15 h

With hydrogenchloride; n-butyllithium; bis-(2-methoxyethoxy)aluminium hydride; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; methanesulfonyl chloride; triethylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; diethyl ether; ethyl acetate; toluene;
DOI:10.1021/jo980396l

Reference yield:

: 211614-45-8
(1R,2R,3E)-5-(tert-butyldiphenylsilyloxy)-1-methoxymethoxy-1-phenyl-pent-3-ene-2-ol

: 211614-51-6
(2S,5R)-2-Hydroxymethyl-5-phenyl-pyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) NaH / 1.) Et₂O, -5 deg C to 23 deg C, 2.) xylene, reflux, 6 h

2: 80 percent / n-Bu₄NF / tetrahydrofuran / 12 h

3: 97 percent / H₂ / PtO₂ / ethyl acetate / 5 h / 23 °C / 760 Torr

4: 92 percent / conc. HCl / methanol / 30 h / 40 °C

5: 60 percent / Et₃N, MsCl / tetrahydrofuran / 48 h / 23 °C

6: 1.) n-BuLi / 1.) THF, hexane, 0 deg C, 30 min, 2.) THF, reflux, 15 h

With hydrogenchloride; n-butyllithium; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; methanesulfonyl chloride; triethylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1021/jo980396l