2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside

Base Information

Chemical Name:2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside
CAS No.:1384442-70-9
Molecular Formula:C₃₈H₄₂O₅S
Molecular Weight:610.814
Hs Code.:

Synonyms:2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside

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Chemical Property of 2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside

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Technology Process of 2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside

There total 4 articles about 2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-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:

: 1384442-64-1
5-tert-butyl-2-methylphenyl 4-O-benzyl-2-O-benzoyl-1-thio-α-L-rhamnopyranoside

: 1384442-70-9
2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium methylate / methanol / 1 h / 20 °C

2.1: di(n-butyl)tin oxide / methanol / 6 h / Reflux; Inert atmosphere

2.2: 48 h / 90 °C

3.1: pyridine / 12 h / 0 - 20 °C

With sodium methylate; di(n-butyl)tin oxide; In pyridine; methanol;
DOI:10.1016/j.carres.2012.01.007

Reference yield:

: 1384442-76-5
2-methyl-5-tert-butylphenyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-1-thio-α-L-rhamnopyranoside

: 1384442-70-9
2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetyl chloride / methanol; dichloromethane / 4 h / 20 °C

2.1: sodium methylate / methanol / 1 h / 20 °C

3.1: di(n-butyl)tin oxide / methanol / 6 h / Reflux; Inert atmosphere

3.2: 48 h / 90 °C

4.1: pyridine / 12 h / 0 - 20 °C

With sodium methylate; di(n-butyl)tin oxide; acetyl chloride; In pyridine; methanol; dichloromethane;
DOI:10.1016/j.carres.2012.01.007

Reference yield:

: 1384442-67-4
2-methyl-5-tert-butylphenyl 4-O-benzyl-1-thio-α-L-rhamnopyranoside

: 1384442-70-9
2-methyl-5-tert-butylphenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1.1: di(n-butyl)tin oxide / methanol / 6 h / Reflux; Inert atmosphere

1.2: 48 h / 90 °C

2.1: pyridine / 12 h / 0 - 20 °C

With di(n-butyl)tin oxide; In pyridine; methanol;
DOI:10.1016/j.carres.2012.01.007