p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside

Base Information

Chemical Name:p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside
CAS No.:99694-46-9
Molecular Formula:C₂₇H₃₈O₁₄
Molecular Weight:586.59
Hs Code.:

Synonyms:p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside

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Chemical Property of p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside

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Technology Process of p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside

There total 9 articles about p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-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:

: 5597-50-2
3-(4-hydroxyphenyl)propionic acid methyl ester

: 99694-46-9
p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: mercury cyanide / acetonitrile / Ambient temperature

2: 1) sodium methoxide / 1) methanol; 2) acetone, 5h

3: mercury cyanide / acetonitrile / Ambient temperature

5: acetic acid, water / methanol / 0.17 h / Heating

With water; sodium methylate; mercury(II) cyanide; acetic acid; In methanol; acetonitrile;

Reference yield:

: 69980-52-5
2,3,4-tri-O-acetyl-L-rhamnopyranosyl bromide

: 99694-46-9
p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: mercury cyanide / acetonitrile / Ambient temperature

2: 1) sodium methoxide / 1) methanol; 2) acetone, 5h

3: mercury cyanide / acetonitrile / Ambient temperature

5: acetic acid, water / methanol / 0.17 h / Heating

With water; sodium methylate; mercury(II) cyanide; acetic acid; In methanol; acetonitrile;

Reference yield:

: 2,4,6-tri-O-acetyl-3-O-methyl-D-glucosyl bromide

: 99694-46-9
p-(2-methoxycarbonylethyl)phenyl 4-O-(2,4-di-O-acetyl-3-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: mercury cyanide / acetonitrile / Ambient temperature

3: acetic acid, water / methanol / 0.17 h / Heating

With water; mercury(II) cyanide; acetic acid; In methanol; acetonitrile;