methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside

Base Information

• Chemical Name: methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside
• CAS No.: 144993-44-2
• Molecular Formula: C₁₄H₁₈O₃
• Molecular Weight: 234.295
• Mol file: 144993-44-2.mol

Synonyms:methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside

Chemical Property of methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside

There total 6 articles about methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside 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: 86.0%

methyl 4-O-benzyl-6-deoxy-2,3-di-O-(methylthio)thiocarbonyl-α-D-mannopyranoside (144872-94-6) → methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside (144993-44-2)

Guidance literature:

With 2,2'-azobis(isobutyronitrile); diphenylsilane; In toluene; for 4h; Heating;

Reference yield:

methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside (109526-95-6) → methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside (144993-44-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) NaH, 2.) imidazole

2: 86 percent / diphenylsilane, AIBN / toluene / 4 h / Heating

With 1H-imidazole; 2,2'-azobis(isobutyronitrile); diphenylsilane; sodium hydride; In toluene;

Reference yield:

benzyl chloride (100-44-7) → methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside (144993-44-2)

Guidance literature:

Multi-step reaction with 4 steps

1: KOH / dimethylsulfoxide / 1.5 h / Ambient temperature

2: 96 percent / methanolic HCl / 4 h / 30 °C

3: 1.) NaH, 2.) imidazole

4: 86 percent / diphenylsilane, AIBN / toluene / 4 h / Heating

With 1H-imidazole; hydrogenchloride; potassium hydroxide; 2,2'-azobis(isobutyronitrile); diphenylsilane; sodium hydride; In dimethyl sulfoxide; toluene;

upstream raw materials:

methyl 4-O-benzyl-6-deoxy-2,3-di-O-(methylthio)thiocarbonyl-α-D-mannopyranoside

methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside

benzyl chloride

methyl 4-O-benzyl-6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside

Downstream raw materials:

methyl 2,3,6-trideoxy-α-D-erythro-hexopyranoside

methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hexopyranoside