4-trityloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole

Base Information

Chemical Name:4-trityloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole
CAS No.:909028-72-4
Molecular Formula:C₃₆H₃₇N₃O₁₀
Molecular Weight:671.704
Hs Code.:

Synonyms:4-trityloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole

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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 4-trityloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole

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Technology Process of 4-trityloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole

There total 1 articles about 4-trityloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole 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: 90.0%

: 76-83-5
trityl chloride

: 70429-41-3
4-hydroxymethyl-1-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole

: 909028-72-4
4-trityloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole

Guidance literature:: With pyridine; at 40 ℃; for 24h;
DOI:10.1016/j.tet.2006.06.001

Reference yield:

: 909028-72-4
4-trityloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole

: 909028-75-7
4-benzoyloxymethyl-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / camphorsulfonic acid / methanol; CH₂Cl₂ / 1 h / 40 °C

2: 88 percent / Et₃N / CH₂Cl₂ / 2 h / 20 °C

With camphor-10-sulfonic acid; triethylamine; In methanol; dichloromethane;
DOI:10.1016/j.tet.2006.06.001