2,3-dinitrophenyl β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-3)-β-D-glucopyranoside

Base Information

Chemical Name:2,3-dinitrophenyl β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-3)-β-D-glucopyranoside
CAS No.:215776-10-6
Molecular Formula:C₂₄H₃₄N₂O₂₀
Molecular Weight:670.535
Hs Code.:

Synonyms:2,3-dinitrophenyl β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-3)-β-D-glucopyranoside

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Chemical Property of 2,3-dinitrophenyl β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-3)-β-D-glucopyranoside

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Technology Process of 2,3-dinitrophenyl β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-3)-β-D-glucopyranoside

There total 3 articles about 2,3-dinitrophenyl β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-3)-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:

: 84396-27-0
(2,3,4,6-tetra-O-acetyl-β-D-glucoyranosyl)-(1-4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1-3)-2,4,6-tri-O-acetyl-α-D-glucopyranosyl bromide

: 215776-10-6
2,3-dinitrophenyl β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-3)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: triethylbenzylammonium bromide, 5 percent NaOH / CH₂Cl₂ / 5 h / Heating

2: NaOMe, MeOH / Ambient temperature

With methanol; sodium hydroxide; sodium methylate; benzyltriethylammonium bromide; In dichloromethane;
DOI:10.1016/S0008-6215(98)00175-X

Reference yield:

: 215775-94-3
(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->3)-1,2,4,6-tetra-O-acetyl-D-glucopyranose

: 215776-10-6
2,3-dinitrophenyl β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-3)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / HBr / 0.5 h / Ambient temperature

2: triethylbenzylammonium bromide, 5 percent NaOH / CH₂Cl₂ / 5 h / Heating

3: NaOMe, MeOH / Ambient temperature

With methanol; sodium hydroxide; hydrogen bromide; sodium methylate; benzyltriethylammonium bromide; In dichloromethane;
DOI:10.1016/S0008-6215(98)00175-X