Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid

Base Information

Chemical Name:Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid
CAS No.:80153-09-9
Molecular Formula:C₄₉H₅₄O₁₀
Molecular Weight:802.962
Hs Code.:

Synonyms:Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid

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Chemical Property of Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid

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Technology Process of Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid

There total 6 articles about Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid 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:

: 4613-15-4
benzyl 4-O-benzyl-α-L-rhamnopyranoside

: 80153-09-9
Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / p-toluenesulphonic acid / toluene / 2 h / Ambient temperature

2: 70 percent / aq. acetic acid / 1 h / Ambient temperature

3: 1) molecular sieve 3 Angstroem / 1) Ag-silicate / 1) CH₂Cl₂, r.t., 2) CH₂Cl₂, -15 deg C

With 3 A molecular sieve; toluene-4-sulfonic acid; Ag-silicate; In acetic acid; toluene;

Reference yield:

: 210426-02-1
2,3,4-tri-O-benzyl-L-rhamnopyranose

: 80153-09-9
Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / pyridine / 12 h / Ambient temperature

2: 98 percent / HBr / CH₂Cl₂ / 0.07 h

3: 1) molecular sieve 3 Angstroem / 1) Ag-silicate / 1) CH₂Cl₂, r.t., 2) CH₂Cl₂, -15 deg C

With 3 A molecular sieve; hydrogen bromide; Ag-silicate; In pyridine; dichloromethane;

Reference yield:

: 80153-03-3
Benzyl-4-O-benzyl-2,3-O-(methyl-orthoacetyl)-α-L-rhamnopyranosid

: 80153-09-9
Benzyl-2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / aq. acetic acid / 1 h / Ambient temperature

2: 1) molecular sieve 3 Angstroem / 1) Ag-silicate / 1) CH₂Cl₂, r.t., 2) CH₂Cl₂, -15 deg C

With 3 A molecular sieve; Ag-silicate; In acetic acid;