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3,4:5,6-di-O-isopropylidene-2-O-(trifluoromethylsulfonyl)-aldehydo-D-glucose dibenzyl acetal

Base Information
  • Chemical Name:3,4:5,6-di-O-isopropylidene-2-O-(trifluoromethylsulfonyl)-aldehydo-D-glucose dibenzyl acetal
  • CAS No.:90597-30-1
  • Molecular Formula:C27H33F3O9S
  • Molecular Weight:590.615
  • Hs Code.:
3,4:5,6-di-O-isopropylidene-2-O-(trifluoromethylsulfonyl)-aldehydo-D-glucose dibenzyl acetal

Synonyms:3,4:5,6-di-O-isopropylidene-2-O-(trifluoromethylsulfonyl)-aldehydo-D-glucose dibenzyl acetal

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Chemical Property of 3,4:5,6-di-O-isopropylidene-2-O-(trifluoromethylsulfonyl)-aldehydo-D-glucose dibenzyl acetal
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Technology Process of 3,4:5,6-di-O-isopropylidene-2-O-(trifluoromethylsulfonyl)-aldehydo-D-glucose dibenzyl acetal

There total 3 articles about 3,4:5,6-di-O-isopropylidene-2-O-(trifluoromethylsulfonyl)-aldehydo-D-glucose dibenzyl acetal 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:
Guidance literature:
Multi-step reaction with 3 steps
1: p-toluensulfonic acid / dioxane / 2 h / Ambient temperature
2: Na-methoxide / methanol
3: 93 percent / pyridine / CH2Cl2 / 1.5 h / -15 - 0 °C
With pyridine; sodium methylate; toluene-4-sulfonic acid; In 1,4-dioxane; methanol; dichloromethane;
DOI:10.1016/0008-6215(84)85111-3
Guidance literature:
Multi-step reaction with 2 steps
1: Na-methoxide / methanol
2: 93 percent / pyridine / CH2Cl2 / 1.5 h / -15 - 0 °C
With pyridine; sodium methylate; In methanol; dichloromethane;
DOI:10.1016/0008-6215(84)85111-3
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