2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-glucopyranoside

Base Information

Chemical Name:2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-glucopyranoside
CAS No.:1622317-89-8
Molecular Formula:C₃₁H₃₀N₂O₉
Molecular Weight:574.587
Hs Code.:

Synonyms:2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-glucopyranoside

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Chemical Property of 2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-glucopyranoside

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Technology Process of 2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-glucopyranoside

There total 7 articles about 2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-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: 77.0%

: 1125-88-8
benzaldehyde dimethyl acetal

: 1622317-92-3
C₂₄H₂₆N₂O₉

: 1622317-89-8
2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-glucopyranoside

Guidance literature:: With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1002/ejoc.201402392

Reference yield:

: 1125-88-8
benzaldehyde dimethyl acetal

: C₂₄H₂₆N₂O₉

: 1622317-89-8
2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-glucopyranoside

Guidance literature:: With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1080/07328303.2021.1928153

Reference yield:

: 77987-49-6
benzyl 2-hydroxyethylcarbamate

: 1622317-89-8
2-(benzyloxycarbonylamino)ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: boron trifluoride diethyl etherate / 1,2-dichloro-ethane / 16 h / 55 °C

2: sodium methylate / methanol / 1 h / 20 °C

3: toluene-4-sulfonic acid / N,N-dimethyl-formamide / 12 h / 20 °C

With boron trifluoride diethyl etherate; sodium methylate; toluene-4-sulfonic acid; In methanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.201402392