allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-β-D-glucopyranoside

Base Information

Chemical Name:allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-β-D-glucopyranoside
CAS No.:866325-73-7
Molecular Formula:C₅₆H₄₈O₁₆
Molecular Weight:976.988
Hs Code.:

Synonyms:allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-β-D-glucopyranoside

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Chemical Property of allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-β-D-glucopyranoside

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Technology Process of allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-β-D-glucopyranoside

There total 5 articles about allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-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: 67.0%

: 866325-70-4
allyl 2,3,4-tri-O-benzoyl-β-D-glucopyranoside

: 14262-83-0
2,3,4-tri-O-benzoyl-α-D-xylopyranosyl bromide

: 866325-73-7
allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-β-D-glucopyranoside

Guidance literature:: With silver trifluoromethanesulfonate; tetramethylurea; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1016/j.tetasy.2005.06.040

Reference yield:

: 866325-71-5
allyl 6-O-(tert-butyldimethylsilyl)-β-D-glucopyranoside

: 866325-73-7
allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / dimethylformamide / 18 h / 20 °C

2: 0.52 g / aq. HCl / tetrahydrofuran / 12 h / 20 °C

3: 67 percent / tetramethylurea; AgOTf / CH₂Cl₂ / 12 h / 20 °C

With pyridine; hydrogenchloride; silver trifluoromethanesulfonate; tetramethylurea; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tetasy.2005.06.040

Reference yield:

: allyl 2,3,4-tri-O-benzoyl-6-tert-butyldimethylsilyl-β-D-glucopyranoside

: 866325-73-7
allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 0.52 g / aq. HCl / tetrahydrofuran / 12 h / 20 °C

2: 67 percent / tetramethylurea; AgOTf / CH₂Cl₂ / 12 h / 20 °C

With hydrogenchloride; silver trifluoromethanesulfonate; tetramethylurea; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tetasy.2005.06.040