allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside

Base Information

Chemical Name:allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside
CAS No.:262599-20-2
Molecular Formula:C₃₆H₃₇N₃O₉
Molecular Weight:655.704
Hs Code.:

Synonyms:allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside

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Technology Process of allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside

There total 4 articles about allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-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: 91.0%

: 100-39-0
benzyl bromide

: 262599-19-9
allyl 2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside

: 262599-20-2
allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 1h;
DOI:10.1246/bcsj.73.173

Reference yield:

: 7784-55-6,10060-23-8
Tetraacetyl-<2,4-dinitrophenyl>-glucosamin

: 262599-20-2
allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: AcBr; H₂O / CHCl₃ / 1.55 h / 0 - 20 °C

2: 57 percent / Hg(CN)2; HgBr₂ / acetonitrile / 20 °C

3: 0.39 g / NaOMe / methanol / 3 h / 20 °C

4: 91 percent / sodium hydride / dimethylformamide / 1 h / 0 - 20 °C

With Acetyl bromide; water; sodium methylate; mercury(II) cyanide; sodium hydride; mercury dibromide; In methanol; chloroform; N,N-dimethyl-formamide; acetonitrile; 1: Substitution / 2: glycosylation / 3: Deacetylation / 4: Alkylation;
DOI:10.1246/bcsj.73.173

Reference yield:

: 3068-36-8
3,4,6-tri-O-acetyl-2-deoxy-2-(2,4-dinitroanilino)-α-D-glucopyranosyl bromide

: 262599-20-2
allyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 57 percent / Hg(CN)2; HgBr₂ / acetonitrile / 20 °C

2: 0.39 g / NaOMe / methanol / 3 h / 20 °C

3: 91 percent / sodium hydride / dimethylformamide / 1 h / 0 - 20 °C

With sodium methylate; mercury(II) cyanide; sodium hydride; mercury dibromide; In methanol; N,N-dimethyl-formamide; acetonitrile; 1: glycosylation / 2: Deacetylation / 3: Alkylation;
DOI:10.1246/bcsj.73.173