(R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol

Base Information

Chemical Name:(R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol
CAS No.:934356-92-0
Molecular Formula:C₂₂H₂₈O₅
Molecular Weight:372.461
Hs Code.:

Synonyms:(R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol

Suppliers and Price of (R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of (R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol

There total 4 articles about (R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol 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: 100.0%

: 934356-91-9
[(R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethoxy]-tert-butyl-dimethyl-silane

: 934356-92-0
(R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol

Guidance literature:: With tetrabutyl ammonium fluoride;
DOI:10.1039/b504558d

Reference yield:

: 177493-29-7
5-O-(tert-butyldimethylsilyl)2,3-di-O-isopropylidene-D-ribitol

: 934356-92-0
(R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: 69 percent / NaH / dimethylformamide / -78 - -20 °C

2: 95 percent / TBAF / tetrahydrofuran / 20 °C

With tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1002/chem.200600659

Reference yield:

: 217309-46-1
5-(tert-butyldimethylsilyloxy)-2,3-isopropylidenedioxy-D-ribofuranose

: 934356-92-0
(R)-2-Benzyloxy-2-((4R,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / NaBH₄

2: 69 percent / NaH

3: 100 percent / TBAF

With sodium tetrahydroborate; tetrabutyl ammonium fluoride; sodium hydride;
DOI:10.1039/b504558d