methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Base Information

Chemical Name:methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside
CAS No.:187159-78-0
Molecular Formula:C₆₁H₆₀O₁₈
Molecular Weight:1081.14
Hs Code.:

methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Synonyms:methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

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Chemical Property of methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

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Technology Process of methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

There total 3 articles about methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 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:

: 153223-32-6
ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

: 187159-78-0
methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / dimethyl(methylthio)sulfonium triflate, 4 A molecular sieves, Et₃N / CH₂Cl₂ / 2 h / Ambient temperature

2: NaOMe / methanol; CH₂Cl₂

3: 1.) Bu₂SnO, 2.) dimethyl(methylthio)sulfonium triflate, 4 A molecular sieves, Et₃N / 1.) MeOH, reflux, 30 min, 2.) MeOH, CH₂Cl₂, RT, overnight

With 4 A molecular sieve; sodium methylate; di(n-butyl)tin oxide; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; triethylamine; In methanol; dichloromethane;
DOI:10.1016/S0968-0896(96)00168-X

Reference yield:

: 187159-75-7
methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

: 187159-78-0
methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: NaOMe / methanol; CH₂Cl₂

2: 1.) Bu₂SnO, 2.) dimethyl(methylthio)sulfonium triflate, 4 A molecular sieves, Et₃N / 1.) MeOH, reflux, 30 min, 2.) MeOH, CH₂Cl₂, RT, overnight

With 4 A molecular sieve; sodium methylate; di(n-butyl)tin oxide; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; triethylamine; In methanol; dichloromethane;
DOI:10.1016/S0968-0896(96)00168-X

Reference yield:

: 153223-32-6
ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

: 187218-12-8
(2R,4aR,6R,7S,8R,8aS)-6-((2R,4aR,6S,7S,8S,8aR)-7-Benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol

: 187159-78-0
methyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-O-(4,6-O-benzylidene-α-D-mannopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Guidance literature:: With 4 A molecular sieve; di(n-butyl)tin oxide; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; triethylamine; Yield given. Multistep reaction; 1.) MeOH, reflux, 30 min, 2.) MeOH, CH₂Cl₂, RT, overnight;
DOI:10.1016/S0968-0896(96)00168-X