3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose

Base Information

Chemical Name:3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose
CAS No.:148704-59-0
Molecular Formula:C₃₀H₂₈O₉
Molecular Weight:532.547
Hs Code.:

Synonyms:3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose

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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 3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose

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Technology Process of 3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose

There total 1 articles about 3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose 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: 97.0%

: 98-88-4
benzoyl chloride

: 55797-64-3,55797-65-4
1,2-O-isopropylidene-4-C-(hydroxymethyl)-β-L-threo-pento-1,4-furanose

: 148704-59-0
3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose

Guidance literature:: With pyridine; for 5h; Ambient temperature;
DOI:10.1135/cccc19930409

Reference yield:

: 148704-59-0
3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose

: C₂₇H₂₄O₉

Guidance literature:: With formic acid; at 50 ℃; for 2h;
DOI:10.1080/15257779408013221

Reference yield:

: 148704-59-0
3,5-di-O-benzoyl-4-C-benzoyloxymethyl-1,2-O-isopropylidene-β-L-arabinofuranose

: 160533-28-8
9-(2-O-acetyl-3,5-di-O-benzoyl-4-C-benzoyloxymethyl-α-L-arabinofuranosyl)-N⁶-benzoyladenine

Guidance literature:: Multi-step reaction with 2 steps

1: H₂SO₄, AcOH / Ambient temperature

2: SnCl₄ / acetonitrile / Ambient temperature

With sulfuric acid; tin(IV) chloride; acetic acid; In acetonitrile;
DOI:10.1135/cccc19941654