benzyl oleanolate 3β-O-[2-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-di-O-benzylidene-β-D-glucopyranoside]

Base Information

Chemical Name:benzyl oleanolate 3β-O-[2-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-di-O-benzylidene-β-D-glucopyranoside]
CAS No.:1352410-56-0
Molecular Formula:C₇₇H₉₀O₁₅
Molecular Weight:1255.55
Hs Code.:

Synonyms:benzyl oleanolate 3β-O-[2-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-di-O-benzylidene-β-D-glucopyranoside]

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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 benzyl oleanolate 3β-O-[2-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-di-O-benzylidene-β-D-glucopyranoside]

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Technology Process of benzyl oleanolate 3β-O-[2-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-di-O-benzylidene-β-D-glucopyranoside]

There total 1 articles about benzyl oleanolate 3β-O-[2-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-di-O-benzylidene-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: 45.0%

: 1352410-51-5
C₅₀H₆₈O₈

: 161007-95-0
2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyltrichloroacetimidate

: 1352410-56-0
benzyl oleanolate 3β-O-[2-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-di-O-benzylidene-β-D-glucopyranoside]

: 1352410-55-9
benzyl oleanolate 3β-O-[3-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-di-O-benzylidene-β-D-glucopyranoside]

: 1352410-54-8
Benzyl oleanolate 3β-O-[2,3-di-O-(2,3,4-tri-O-benzoyl-α-l-rhamnopyranosyl)-4,6-di-O-benzylid-ene-β-d-glucopyranoside]

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 20 ℃; for 0.166667h; Molecular sieve;
DOI:10.1016/j.ejmech.2013.04.016