2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose

Base Information

Chemical Name:2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose
CAS No.:1415238-58-2
Molecular Formula:C₃₃H₃₉NO₂₁
Molecular Weight:785.667
Hs Code.:

Synonyms:2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose

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Chemical Property of 2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose

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Technology Process of 2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose

There total 1 articles about 2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose 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: 57.0%

: 97-51-8
5-Nitrosalicylaldehyde

: 4753-07-5
2,3,6,2',3',4',6'-hepta-O-acetyl-lactosyl bromide

: 1415238-58-2
2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose

Guidance literature:: With tetrabutylammomium bromide; sodium hydroxide; In dichloromethane; water; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ja309790w

Reference yield: 91.0%

: 1415238-58-2
2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose

: 1415238-59-3
2-difluromethyl-4-nitro 2,3,4,6,2′ ,3′ ,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose

Guidance literature:: With diethylamino-sulfur trifluoride; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ja309790w

Reference yield:

: 1415238-58-2
2-formyl-4-nitro 2,3,4,6,2′ ,3′,4′ ,6′-hepta-O-acetyl-1-phenoxyl-α-D-lactopyranose

: 1415238-60-6
C₃₃H₄₁F₂NO₁₈

Guidance literature:: Multi-step reaction with 2 steps

1: diethylamino-sulfur trifluoride / dichloromethane / 0 - 20 °C / Inert atmosphere

2: palladium 10% on activated carbon; hydrogen / ethyl acetate / 2 h / Inert atmosphere

With diethylamino-sulfur trifluoride; palladium 10% on activated carbon; hydrogen; In dichloromethane; ethyl acetate;
DOI:10.1021/ja309790w