octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

Base Information

Chemical Name:octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside
CAS No.:912364-41-1
Molecular Formula:C₅₃H₆₄Cl₃NO₁₃
Molecular Weight:1029.45
Hs Code.:

octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

Synonyms:octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

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Chemical Property of octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

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Technology Process of octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

There total 6 articles about octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-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: 67.0%

: 912364-38-6
octyl 4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

: 162466-43-5
ethyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside

: 912364-41-1
octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

Guidance literature:: With N-iodo-succinimide; silver trifluoromethanesulfonate; In dichloromethane; at -70 - -50 ℃; for 3h;
DOI:10.1021/jo060485v

Reference yield:

: ((2R,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-octyloxy-tetrahydro-pyran-3-yl)-carbamic acid 2,2,2-trichloro-ethyl ester

: 912364-41-1
octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 3.75 g / camphorsulfonic acid / acetonitrile / 20 °C

2: 67 percent / NIS; AgOTf / CH₂Cl₂ / 3 h / -70 - -50 °C

With N-iodo-succinimide; camphor-10-sulfonic acid; silver trifluoromethanesulfonate; In dichloromethane; acetonitrile;
DOI:10.1021/jo060485v

Reference yield:

: 912364-35-3
octyl 3,4,6-tri-O-acetyl-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

: 912364-41-1
octyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-2-[[(2,2,2-trichloroethoxy)carbonyl]amino]-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: MeONa / methanol / 0 °C

2: 3.75 g / camphorsulfonic acid / acetonitrile / 20 °C

3: 67 percent / NIS; AgOTf / CH₂Cl₂ / 3 h / -70 - -50 °C

With N-iodo-succinimide; camphor-10-sulfonic acid; sodium methylate; silver trifluoromethanesulfonate; In methanol; dichloromethane; acetonitrile;
DOI:10.1021/jo060485v