2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Base Information

Chemical Name:2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
CAS No.:433331-35-2
Molecular Formula:C₂₉H₃₂O₁₂
Molecular Weight:572.566
Hs Code.:

Synonyms:2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

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Chemical Property of 2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Chemical Property:

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Technology Process of 2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

There total 5 articles about 2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 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:

: 433331-27-2
4-(2-hydroxybenzyl)benzoic acid methyl ester

: 604-69-3
β-D-glucose pentaacetate

: 433331-35-2
2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Guidance literature:: In dichloromethane; toluene;

Reference yield:

: 433331-26-1
4-[(2-Benzyloxyphenyl)hydroxymethyl]-benzoic Acid Methyl Ester

: 433331-35-2
2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / 10% palladium on activated carbon / ethanol / 18 h / 20 °C

2: boron trifluoride diethyl etherate / dichloromethane; toluene / 20 °C

With boron trifluoride diethyl etherate; hydrogen; 10% palladium on activated carbon; In ethanol; dichloromethane; toluene;

Reference yield:

: 31575-75-4
2-bromophenyl benzyl ether

: 433331-35-2
2-(4-methoxycarbonylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: magnesium / tetrahydrofuran

2: hydrogenchloride / tetrahydrofuran / 1 h / 20 °C

3: hydrogen / 10% palladium on activated carbon / ethanol / 18 h / 20 °C

4: boron trifluoride diethyl etherate / dichloromethane; toluene / 20 °C

With hydrogenchloride; boron trifluoride diethyl etherate; hydrogen; magnesium; 10% palladium on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; toluene;