N-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide

Base Information

Chemical Name:N-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide
CAS No.:225923-18-2
Molecular Formula:C₄₁H₄₁NO₆
Molecular Weight:643.78
Hs Code.:

Synonyms:N-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide

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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-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide

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Technology Process of N-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide

There total 3 articles about N-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide 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: 74.0%

: 128984-82-7
(2R,3S,4R,5R)-N-benzyl-5-hydroxy-2,3,4,6-tetrabenzyloxyhexanamide

: 225923-18-2
N-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide

Guidance literature:: With acetic anhydride; dimethyl sulfoxide; at 20 ℃; for 15h;
DOI:10.1135/cccc19990673

Reference yield:

: 13096-62-3
(3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one

: 225923-18-2
N-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / toluene / 5 h / Heating

2: 74 percent / DMSO; Ac₂O / 15 h / 20 °C

With acetic anhydride; dimethyl sulfoxide; In toluene; 1: Substitution / 2: Oxidation;
DOI:10.1135/cccc19990673

Reference yield:

: 100-46-9
benzylamine

: 225923-18-2
N-Benzyl-2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / toluene / 5 h / Heating

2: 74 percent / DMSO; Ac₂O / 15 h / 20 °C

With acetic anhydride; dimethyl sulfoxide; In toluene; 1: Substitution / 2: Oxidation;
DOI:10.1135/cccc19990673