methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

Base Information

Chemical Name:methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside
CAS No.:651735-96-5
Molecular Formula:C₂₈H₃₁NO₅
Molecular Weight:461.558
Hs Code.:

Synonyms:methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

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Chemical Property of methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

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Technology Process of methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

There total 6 articles about methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-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:

: 128657-58-9
methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

: 651735-96-5
methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: diisopropylethylamine / CH₂Cl₂ / 12 h / Heating

2: tetrabutylammonium iodide / CH₂Cl₂ / 24 h / Heating

3: 0.9 g / aq. HCl / 0.5 h

With hydrogenchloride; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1039/b309715n

Reference yield:

: 100-39-0
benzyl bromide

: 651735-96-5
methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: tetrabutylammonium iodide / CH₂Cl₂ / 24 h / Heating

2: 0.9 g / aq. HCl / 0.5 h

With hydrogenchloride; tetra-(n-butyl)ammonium iodide; In dichloromethane;
DOI:10.1039/b309715n

Reference yield:

: 651736-08-2
methyl 4,6-O-benzylidene-α-D-arabino-hexopyranoside-2-ulose Z-oxime

: 651735-96-5
methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 36 percent / LiAlH₄; H₂SO₄ / tetrahydrofuran / 5 h / 20 °C

2: diisopropylethylamine / CH₂Cl₂ / 12 h / Heating

3: tetrabutylammonium iodide / CH₂Cl₂ / 24 h / Heating

4: 0.9 g / aq. HCl / 0.5 h

With hydrogenchloride; lithium aluminium tetrahydride; sulfuric acid; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1039/b309715n