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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057227Generated: November 4, 2026

Tetrabutylammonium Fluoride → HCID 86684713, compound

https://huagongshe.com/reaction/1057227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86684714HCID 86684714—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86684713HCID 8668471396.3%

Reaction Steps

To a solution of compound 42 (55 mg, 0.09 mmol) in THF (10 mL), n-Bu4NF (63 mg, 0.20 mmol) was added. The mixture was stirred at room temperature for four hours and concentrated in vacuo, and the residue was purified by silica gel column chromatography to yield 5-(2-nitrobenzyloxyl)methyl-2′-deoxycytidine 43 (34 mg, 96%). 1H NMR (400 MHz, DMSO-d6): δ 8.05 (d, J=8.0 Hz, 1H, Ph-H), 7.89 (s, 1H, H-6), 7.74 (m, 2H, Ph-H), 7.55 (m, 1H, Ph-H), 7.39 (br s, 1H, D2O exchangeable, NH2), 6.74 (br s, 1H, D2O exchangeable, NH2), 6.12 (t, 1H, J=6.4 Hz, H-1′), 5.21 (br s, 1H, D2O exchangeable, 3′-OH), 4.99 (br s, 1H, D2O exchangeable, 5′-OH), 4.81 (s, 2H, Ph-CH2), 4.30 (dd, 2H, J=11.6 Hz, 5-CH2), 4.20 (m, 1H, H-3′), 3.76 (m, 1H, H-4′), 3.55 (m, 2H, H-5′), 2.11 (m, 1H, H-2′a), 1.95 (m, 1H, H-2′b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399798B2
Source datasetuspto-grants-2016_07
ORD IDord-ae9a85ccda0044ff9c42b837950e3ac4
Source noteuspto-grants-2016_07