methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside

Base Information

Chemical Name:methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside
CAS No.:174089-83-9
Molecular Formula:C₄₃H₄₂O₁₅
Molecular Weight:798.797
Hs Code.:

Synonyms:methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside

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Chemical Property of methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside

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Technology Process of methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside

There total 6 articles about methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside 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:

: C₅₀H₄₇IO₁₅

: 174089-83-9
methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside

Guidance literature:: With hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In ethyl acetate; for 48h; under 3000.2 Torr; Yield given;
DOI:10.1016/0008-6215(95)00268-5

Reference yield:

: 14218-11-2,14218-30-5,61198-88-7,108438-33-1,108836-02-8,114682-36-9,127305-34-4,151377-77-4
2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide

: 174089-83-9
methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / silver trifluoromethanesulfonate, 4 Angstroem molecular sieves / toluene; CH₂Cl₂ / -50 - 20 °C

2: pyridine / 40 °C

3: H₂, aq. NaHCO₃ / Pd-C / ethyl acetate / 48 h / 3000.2 Torr

With pyridine; 4 A molecular sieve; hydrogen; silver trifluoromethanesulfonate; sodium hydrogencarbonate; palladium on activated charcoal; In dichloromethane; ethyl acetate; toluene;
DOI:10.1016/0008-6215(95)00268-5

Reference yield:

: 2774-19-8,14419-69-3,15887-67-9,23392-28-1,57539-08-9,61277-63-2,74410-51-8,76419-48-2,80734-73-2,86363-44-2,89301-79-1,94061-92-4,94062-87-0,108739-92-0,129706-93-0,143005-12-3,65877-21-6
(2R,4aR,6S,7S,8R,8aR)-8-Benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

: 174089-83-9
methyl 4-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-arabino-hexopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 77 percent / triiodoimidazole, triphenylphosphine / toluene / Heating

2: 75 percent / 70percent aq. AcOH / 48 h / Ambient temperature

3: 92 percent / silver trifluoromethanesulfonate, 4 Angstroem molecular sieves / toluene; CH₂Cl₂ / -50 - 20 °C

4: pyridine / 40 °C

5: H₂, aq. NaHCO₃ / Pd-C / ethyl acetate / 48 h / 3000.2 Torr

With pyridine; tri-iodoimidazole; 4 A molecular sieve; hydrogen; silver trifluoromethanesulfonate; sodium hydrogencarbonate; acetic acid; triphenylphosphine; palladium on activated charcoal; In dichloromethane; ethyl acetate; toluene;
DOI:10.1016/0008-6215(95)00268-5