benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside

Base Information

• Chemical Name: benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside
• CAS No.: 144296-83-3
• Molecular Formula: C₁₆H₂₂O₅S₂
• Molecular Weight: 358.48
• Mol file: 144296-83-3.mol

Synonyms:benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside

Chemical Property of benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside

There total 4 articles about benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside 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:

(2R,3R,4R,5R,6S)-2-benzyloxy-tetrahydro-6-methyl-2H-pyran-3,4,5-triol (3359-35-1,16741-29-0,71731-74-3,78120-06-6,84911-79-5,84911-80-8,87598-99-0,87599-00-6,88818-92-2,97133-57-8,114298-06-5,127000-09-3) → benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside (144296-83-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) dibutylstannoxane / 1.) toluene, reflux, 1 h, 2.) THF, RT, 2 h

2: 1.) NaH

With dibutylstannoxane; sodium hydride;

DOI:10.1080/00397919208021642

Reference yield:

L-rhamnose (6014-42-2) → benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside (144296-83-3)

Guidance literature:

Multi-step reaction with 3 steps

1: acetyl chloride / 5 h / Ambient temperature

2: 1.) dibutylstannoxane / 1.) toluene, reflux, 1 h, 2.) THF, RT, 2 h

3: 1.) NaH

With dibutylstannoxane; sodium hydride; acetyl chloride;

DOI:10.1080/00397919208021642

Reference yield:

benzyl alcohol (100-51-6,185532-71-2) → benzyl 3-O-methyl-2-O-(thiomethoxythiocarbonyl)-α-L-rhamnopyranoside (144296-83-3)

Guidance literature:

Multi-step reaction with 3 steps

1: acetyl chloride / 5 h / Ambient temperature

2: 1.) dibutylstannoxane / 1.) toluene, reflux, 1 h, 2.) THF, RT, 2 h

3: 1.) NaH

With dibutylstannoxane; sodium hydride; acetyl chloride;

DOI:10.1080/00397919208021642

upstream raw materials:

carbon disulfide

benzyl 3-O-methyl-α-L-rhamnopyranoside

methyl iodide

L-rhamnose

Downstream raw materials:

benzyl 2-deoxy-3-O-methyl-α-L-rhamnopyranoside