(2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride

Base Information

• Chemical Name: (2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride
• CAS No.: 144397-81-9
• Molecular Formula: C₁₃H₁₉NO₄*ClH
• Molecular Weight: 289.759
• Mol file: 144397-81-9.mol

Synonyms:(2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride

Chemical Property of (2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride

There total 3 articles about (2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride 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: 98.0%

2,5-dideoxy-2,5-N-benzylimino-1,3:4,6-di-O-benzylidene-L-iditol (144266-28-4,1144513-20-1) → (2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride (144397-81-9)

Guidance literature:

With hydrogenchloride; In methanol; for 48h; Ambient temperature;

DOI:10.1016/S0040-4039(00)61197-8

Reference yield:

1,3:4,6-di-O-benzylidene-D-mannitol (28224-73-9) → (2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride (144397-81-9)

Guidance literature:

Multi-step reaction with 3 steps

1: Et₃N / CH₂Cl₂ / 2 h / 0 °C

2: 94 percent / 8 h / 135 °C

3: 98 percent / conc.HCl / methanol / 48 h / Ambient temperature

With hydrogenchloride; triethylamine; In methanol; dichloromethane;

DOI:10.1016/S0040-4039(00)61197-8

Reference yield:

1,3:4,6-di-O-benzylidene-2,5-di-O-methanesulfonyl-D-mannitol (28224-74-0) → (2S,3R,4R,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol; hydrochloride (144397-81-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 94 percent / 8 h / 135 °C

2: 98 percent / conc.HCl / methanol / 48 h / Ambient temperature

With hydrogenchloride; In methanol;

DOI:10.1016/S0040-4039(00)61197-8

upstream raw materials:

2,5-dideoxy-2,5-N-benzylimino-1,3:4,6-di-O-benzylidene-L-iditol

1,3:4,6-di-O-benzylidene-D-mannitol

1,3:4,6-di-O-benzylidene-2,5-di-O-methanesulfonyl-D-mannitol

Downstream raw materials:

(2S,3R,4R,5S)-1-Benzyl-3,4-dimethoxy-2,5-bis-methoxymethyl-pyrrolidine

(2S,3R,4R,5S)-3,4-dihydroxy-2,5-bis(hydroxymethyl)pyrrolidine

(2S,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-2,5-bis-benzyloxymethyl-pyrrolidine