[(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol

Base Information

• Chemical Name: [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol
• CAS No.: 857732-38-8
• Molecular Formula: C₁₄H₂₀O₅
• Molecular Weight: 268.31
• Mol file: 857732-38-8.mol

Synonyms:[(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol

Chemical Property of [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol

There total 1 articles about [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol 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:

C33H34O5 → [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol (857732-38-8) + C14H20O5

Guidance literature:

With hydrogenchloride; In methanol;

DOI:10.1039/b708594j

Reference yield:

[(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol (857732-38-8) → (2S,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-carboxylic acid

Guidance literature:

With 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; sodium chlorite;

DOI:10.1039/b504258e

Reference yield:

[(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol (857732-38-8) → (2S,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-carboxylic acid allyl ester (857732-39-9)

Guidance literature:

Multi-step reaction with 2 steps

1: NaOCl; NaClO₂; TEMPO

2: DCC; DMAP

With dmap; 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; sodium chlorite; dicyclohexyl-carbodiimide;

DOI:10.1039/b504258e

Downstream raw materials:

(2S,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-carboxylic acid allyl ester