ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

Base Information

Chemical Name:ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside
CAS No.:653597-45-6
Molecular Formula:C₄₄H₅₀O₉S
Molecular Weight:754.942
Hs Code.:

Synonyms:ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

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Chemical Property of ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

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Technology Process of ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

There total 4 articles about ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-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: 87.0%

: 100-39-0
benzyl bromide

: 653597-44-5
ethyl (β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

: 653597-45-6
ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 1h;
DOI:10.1081/CAR-120026459

Reference yield:

: 142924-31-0
S-ethyl 4,6-O-benzylidene-1-thio-α-D-mannopyranoside

: 653597-45-6
ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1.1: Bu₂SnO / methanol / 1 h / Heating

1.2: 86 percent / CsF / dimethylformamide / 20 °C

2.1: silver triflate; 2,6-di-tert-butylpyridine; molecular sieves 4 Angstroem / CH₂Cl₂; toluene / 1 h / -40 °C

2.2: Et₃N / toluene; CH₂Cl₂ / 0.25 h / -40 °C

3.1: 3.37 g / NaOMe / methanol / 4 h / 20 °C

4.1: 87 percent / NaH / dimethylformamide / 1 h / 0 °C

With 2,6-di-tert-butyl-pyridine; 4 A molecular sieve; sodium methylate; silver trifluoromethanesulfonate; sodium hydride; di(n-butyl)tin oxide; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1081/CAR-120026459

Reference yield:

: 319922-00-4
ethyl 3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

: 653597-45-6
ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: silver triflate; 2,6-di-tert-butylpyridine; molecular sieves 4 Angstroem / CH₂Cl₂; toluene / 1 h / -40 °C

1.2: Et₃N / toluene; CH₂Cl₂ / 0.25 h / -40 °C

2.1: 3.37 g / NaOMe / methanol / 4 h / 20 °C

3.1: 87 percent / NaH / dimethylformamide / 1 h / 0 °C

With 2,6-di-tert-butyl-pyridine; 4 A molecular sieve; sodium methylate; silver trifluoromethanesulfonate; sodium hydride; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1081/CAR-120026459