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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689622Generated: October 30, 2026

Tetrabutylammonium Fluoride → 8-(3-Pyridinyl)adenosine

https://huagongshe.com/reaction/1689622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2',3',5'-Tris-o-(tert-butyldimethylsilyl)-8-(3-pyridinyl)adenosineHCID 66906775—
SolventTetrahydrofuranHCID 8028—
Product8-(3-Pyridinyl)adenosineHCID 66906425—

Reaction Steps

A solution of 2′,3′,5′-tris-O-(tert-butyldimethylsilyl)-8-(3-pyridinyl)adenosine (16c) (0.56 g, 0.82 mmol) and TBAF (0.85 g, 3.26 mmol) in THF (31 ml) under argon was stirred at room temperature overnight. The solvent was distilled off and the residual material dissolved in MeOH (10 ml). The solution was left at 0° C. overnight and the title compound isolated by filtration. 13C NMR: (75 MHz, DMSO); δ 62.27 (C-5′), 71.13/71.62 (C-2′, C-3′), 86.95/89.27 (C-4, C-1), 119.33/123.69/125.71/137.20/148.20/149.80/149.85/150.88/152.33/156.34 (C-5, C-5″, C-3″, C-4″, C-6, C-8, C-6″, C-2″, C-2, C-4). MS (EI): 344 (M, 2%), 255 (5), 241 (5), 213 (22), 212 (100), 211 (5) 185 (12), 104 (12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153609B2
Source datasetuspto-grants-2012_04
ORD IDord-2feb1e3ce04442feaeb3e05f54cb03dc
Source noteuspto-grants-2012_04