methyl 3,6-di-O-benzoyl-2-deoxy-2-(N-hydroxy-N-3,7-dimethyloct-6-enylamino)-α-D-arabino-hexopyranosid-4-ulose

Base Information

• Chemical Name: methyl 3,6-di-O-benzoyl-2-deoxy-2-(N-hydroxy-N-3,7-dimethyloct-6-enylamino)-α-D-arabino-hexopyranosid-4-ulose
• CAS No.: 129192-81-0
• Molecular Formula: C₃₁H₃₉NO₈
• Molecular Weight: 553.653
• Mol file: 129192-81-0.mol

Synonyms:methyl 3,6-di-O-benzoyl-2-deoxy-2-(N-hydroxy-N-3,7-dimethyloct-6-enylamino)-α-D-arabino-hexopyranosid-4-ulose

Chemical Property of methyl 3,6-di-O-benzoyl-2-deoxy-2-(N-hydroxy-N-3,7-dimethyloct-6-enylamino)-α-D-arabino-hexopyranosid-4-ulose

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 3,6-di-O-benzoyl-2-deoxy-2-(N-hydroxy-N-3,7-dimethyloct-6-enylamino)-α-D-arabino-hexopyranosid-4-ulose

There total 2 articles about methyl 3,6-di-O-benzoyl-2-deoxy-2-(N-hydroxy-N-3,7-dimethyloct-6-enylamino)-α-D-arabino-hexopyranosid-4-ulose 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%

((2R,6S)-4-(benzoyloxy)-6-methoxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)methyl benzoate (25552-06-1) + N-(3,7-dimethyloct-6-enyl)hydroxylamine (129192-82-1) → methyl 3,6-di-O-benzoyl-2-deoxy-2-(N-hydroxy-N-3,7-dimethyloct-6-enylamino)-α-D-arabino-hexopyranosid-4-ulose (129192-81-0)

Guidance literature:

In tetrahydrofuran; at 25 ℃; for 2h;

DOI:10.1016/0008-6215(90)84212-D

Reference yield:

rac-3,7-dimethyloct-6-enenitrile oxime (22457-25-6) → methyl 3,6-di-O-benzoyl-2-deoxy-2-(N-hydroxy-N-3,7-dimethyloct-6-enylamino)-α-D-arabino-hexopyranosid-4-ulose (129192-81-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 56 percent / sodium cyanoborohydride

2: 86 percent / tetrahydrofuran / 2 h / 25 °C

With sodium cyanoborohydride; In tetrahydrofuran;

DOI:10.1016/0008-6215(90)84212-D

upstream raw materials:

((2R,6S)-4-(benzoyloxy)-6-methoxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)methyl benzoate

N-(3,7-dimethyloct-6-enyl)hydroxylamine

rac-3,7-dimethyloct-6-enenitrile oxime