3-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose

Base Information

Chemical Name:3-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose
CAS No.:945621-31-8
Molecular Formula:C₂₁H₃₄O₅Si
Molecular Weight:394.583
Hs Code.:

Synonyms:3-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose

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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-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose

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Technology Process of 3-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose

There total 1 articles about 3-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose 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: 85.0%

: 1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose

: 100-39-0
benzyl bromide

: 945621-31-8
3-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1080/07328300701351532

Reference yield: 85.0%

: 945621-31-8
3-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose

: 679394-50-4
3-O-benzyl-1,2-O-isopropylidene-α-L-ribofuranose

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1080/07328300701351532

Reference yield:

: 945621-31-8
3-O-benzyl-1,2-O-isopropylidene-5-O-tert-butyldimethylsilyl-α-L-ribofuranose

: 945621-65-8
C₁₆H₁₉O₇SF₃

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / tetrabutylammonium fluoride / tetrahydrofuran / 2 h / 20 °C

2: 95 percent / 2,6-lutidine / CH₂Cl₂ / 2 h / -30 °C

With 2,6-dimethylpyridine; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane;
DOI:10.1080/07328300701351532