3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose

Base Information

Chemical Name:3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose
CAS No.:1380315-47-8
Molecular Formula:C₄₃H₄₄O₇
Molecular Weight:672.818
Hs Code.:

Synonyms:3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose

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Chemical Property of 3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose

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Technology Process of 3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose

There total 5 articles about 3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose 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:

: 37073-70-4
1-(6-benzyloxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)-2-trityloxyethanol

: 1380315-47-8
3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 20 ℃; for 10h;
DOI:10.1002/ejoc.201101815

Reference yield:

: 22529-61-9
(1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol

: 1380315-47-8
3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 0 - 20 °C

2: tetra-(n-butyl)ammonium iodide; sodium hydride / N,N-dimethyl-formamide; mineral oil / 10 h / 20 °C

With pyridine; tetra-(n-butyl)ammonium iodide; sodium hydride; In N,N-dimethyl-formamide; mineral oil;
DOI:10.1002/ejoc.201101815

Reference yield:

: 100-39-0
benzyl bromide

: 1380315-47-8
3-O-benzyl-5-O-(4-methoxybenzyl)-6-O-triphenylmethyl-1,2-O-isopropylidene-α-D-glucofuranose

Guidance literature:: Multi-step reaction with 4 steps

1: tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 8 h / 20 °C

2: acetic acid / water / 2 h / 80 °C

3: pyridine / 0 - 20 °C

4: tetra-(n-butyl)ammonium iodide; sodium hydride / N,N-dimethyl-formamide; mineral oil / 10 h / 20 °C

With pyridine; tetra-(n-butyl)ammonium iodide; sodium hydride; acetic acid; In water; N,N-dimethyl-formamide; mineral oil;
DOI:10.1002/ejoc.201101815