N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Base Information

Chemical Name:N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
CAS No.:98911-16-1
Molecular Formula:C₂₈H₂₉Cl₂NO₁₂
Molecular Weight:642.444
Hs Code.:

Synonyms:N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-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 N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

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Technology Process of N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

There total 4 articles about N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-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: 29.0%

: 98911-12-7
3,4,6-tri-O-acetyl-1,2-O-<1-ethylidene>-α-D-glucopyranose

: 98911-16-1
N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Guidance literature:: 2,6-lutidinium perchlorate; In various solvent(s); for 25h; Heating;

Reference yield: 16.0%

: 98911-08-1
2,4-Dichloro-4'-hydroxyacetylaminobiphenyl ether

: 572-09-8
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

: 98911-16-1
N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Guidance literature:: With silver carbonate; In benzene; for 24h; Ambient temperature;

Reference yield:

: 1836-75-5
nitrofen

: 98911-16-1
N-acetyl-4-(2,4-dichlorophenoxy)anilino 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) aq. ammonium chloride, zinc 2.) sodium hydrogen carbonate / 1.) dioxane, 15 min 2.) ether, water, 1.5 h

2: 80 percent / 2,6-lutidine / nitromethane / 42 h / 37 °C / in the dark

3: 29 percent / 2,6-lutidinium perchlorate / various solvent(s) / 25 h / Heating

With 2,6-dimethylpyridine; ammonium chloride; sodium hydrogencarbonate; zinc; 2,6-lutidinium perchlorate; In nitromethane;