allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside

Base Information

Chemical Name:allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside
CAS No.:273384-27-3
Molecular Formula:C₃₆H₄₄O₁₀
Molecular Weight:636.739
Hs Code.:

Synonyms:allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside

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Technology Process of allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside

There total 3 articles about allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside 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: 70.0%

: 273384-26-2
allyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside

: 273384-27-3
allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside

Guidance literature:: With sodium methylate; In methanol; at 20 ℃; for 24h;
DOI:10.1016/S0008-6215(99)00315-8

Reference yield:

: 113893-72-4
2,3,4-tri-O-acetyl-L-rhamnopyranosyl trichloroacetimidate

: 273384-27-3
allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / 4 Angstroem mol. sieves; silver triflate / CH₂Cl₂ / 24 h / 20 °C

2: 70 percent / NaOMe / methanol / 24 h / 20 °C

With 4 A molecular sieve; sodium methylate; silver trifluoromethanesulfonate; In methanol; dichloromethane; 1: Etherification / 2: Deacetylation;
DOI:10.1016/S0008-6215(99)00315-8

Reference yield:

: 150969-29-2
allyl 2,3,6-tri-O-benzyl-β-D-galactopyranoside

: 273384-27-3
allyl α-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / 4 Angstroem mol. sieves; silver triflate / CH₂Cl₂ / 24 h / 20 °C

2: 70 percent / NaOMe / methanol / 24 h / 20 °C

With 4 A molecular sieve; sodium methylate; silver trifluoromethanesulfonate; In methanol; dichloromethane; 1: Etherification / 2: Deacetylation;
DOI:10.1016/S0008-6215(99)00315-8