Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288279Generated: November 2, 2026

Tetrabutylammonium Fluoride → 3'-[(Acetyloxy)methyl]-3'-deoxythymidine

https://huagongshe.com/reaction/2288279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 21969455HCID 21969455—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3'-[(Acetyloxy)methyl]-3'-deoxythymidineHCID 2196945257%

Reaction Steps

Compound 183 (2.00 g, 3.73 mmol) was dissolved in dry THF (36 ml) and tetrabutylammonium fluoride (8.8 ml, 1.0 M solution in THF, 2.4 equiv.) was added via syringe at room temperature under an atmosphere of argon. After completion of the reaction (1.5 hours), as was monitored by tlc in EtOAc (Rf 0.42), the solvent was removed in vacuo. The residue was purified by silica gel flash column chromatography in EtOAc/Hexane (4:6-9:1, v/v) to afford 184 (0.63 g, 57%) 1H NMR (CDCl3): δ8.89 (br, 1 H, NH), 7.55 (d, 1 H, J=1.1 Hz, H6), 6.13 (dd, 1 H, J=4.9, 6.6 Hz, H-1'), 4.17 & 4.09 (m, 2 H, CH2 -OAc), 4.07 (d, 1 H, J=11.7 Hz, H-5' & H-5'), 3.94-3.90 (m, 1 H, H-4'), 3.76 (d, 1H, J=11.7 Hz, H-5), 2.80-2.76 (m, 1 H, H-3'), 2.60 (br, 1 H, OH), 2.29-2.25 (m, 2 H, H2' & H-2"), 2.09 (s, 3 H, COCH3), 1.91 (s, 9 H, C(CH3)3); 13C NMR (CDCl3): 170.8 (C=O), 163.8 (C4), 150.3 (C2), 136.3 (C6), 110.8 (C5), 85.4 (C1'), 83.5 (C4'), 64.2 (C5'), 36.8 (C3'), 35 35.6 (C2'), 20.8, 12.5;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087482
Source datasetuspto-grants-2000_07
ORD IDord-5fa0a808d94748b3bf096bcd1495aa89
Source noteuspto-grants-2000_07