(2S,4S)-4-methoxypyrrolidine-2-carboxylic acid

Base Information

• Chemical Name: (2S,4S)-4-methoxypyrrolidine-2-carboxylic acid
• CAS No.: 75176-22-6
• Molecular Formula: C6H11NO3
• Molecular Weight: 145.158
• European Community (EC) Number: 817-968-2
• Mol file: 75176-22-6.mol

Synonyms:(2S,4S)-4-methoxypyrrolidine-2-carboxylic acid;75176-22-6;cis-4-methoxy-L-proline;SCHEMBL1269918;RNXKXUOGQKYKTH-WHFBIAKZSA-N;AKOS006353411;(2S,4S)-4-methoxypyrrolidine-2-carboxylicacid;EN300-657362;Z1203733743

Chemical Property of (2S,4S)-4-methoxypyrrolidine-2-carboxylic acid

Chemical Property:

• PSA: 58.56000
• LogP: -0.22330
• XLogP3: -2.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 145.07389321
• Heavy Atom Count: 10
• Complexity: 137

Purity/Quality:

97% ^*data from raw suppliers

(2S,4S)-4-Methoxypyrrolidine-2-carboxylicacid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1CC(NC1)C(=O)O
• Isomeric SMILES: CO[C@H]1C[C@H](NC1)C(=O)O

Technology Process of (2S,4S)-4-methoxypyrrolidine-2-carboxylic acid

There total 3 articles about (2S,4S)-4-methoxypyrrolidine-2-carboxylic acid 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: 93.0%

N-(benzyloxycarbonyl)-cis-4-methoxy-L-proline (75176-20-4) → cis-4-methoxy-L-proline (75176-22-6)

Guidance literature:

With hydrogen; In methanol; water; under 2280 Torr;

DOI:10.1021/jm00401a014

Reference yield:

(2S,4S)-1-benzyloxycarbonyl-4-hydroxyproline (13504-86-4) → cis-4-methoxy-L-proline (75176-22-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) silver(I) oxide, 2.) 1N KOH / 1.) acetone, overnight

2: 93 percent / H₂ / methanol; H₂O / 2280 Torr

With potassium hydroxide; hydrogen; silver(l) oxide; In methanol; water;

DOI:10.1021/jm00401a014

Reference yield:

→ cis-4-methoxy-L-proline (75176-22-6)

Guidance literature:

cis-1-Acetyl-4-methoxy-pyrrolidin-carbonsaeure-(2)-methylester, wss. Ba(OH)2;

upstream raw materials:

N-(benzyloxycarbonyl)-cis-4-methoxy-L-proline

(2S,4S)-1-benzyloxycarbonyl-4-hydroxyproline

Downstream raw materials:

(2S,4S)-1-{2-[Hydroxy-(4-phenyl-butyl)-phosphinoyl]-acetyl}-4-methoxy-pyrrolidine-2-carboxylic acid