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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249056Erstellt: 24. Oktober 2026

p-Toluenesulfonic acid → 2',3'-Didehydro-2',3'-dideoxyuridine

https://huagongshe.com/de/reaction/249056

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktSodium HydroxideHCID 14798—
Edukt5'O-trityl-2',3'-dideoxy-2',3'-didehydrouridineHCID 11091653—
LösungsmittelMethanolHCID 887—
LösungsmittelChloroformHCID 6212—
Produkt2',3'-Didehydro-2',3'-dideoxyuridineHCID 65159—

Reaktionsschritte

5'O-trityl-2',3'-dideoxy-2',3'-didehydrouridine (0.5 gm.,1.1 mM) was dissolved in a chloroform (10 mL) and methanol (2 mL) mixture containing 2% p-toluenesulphonic acid. The reaction mixture was stirred at room temperature for 0.75 hr., and then neutralized with 2N NaOH (0.5 mL). The solvent was removed in vacuo and the residue chromatographed on silica using chloroform/acetone (2:1) as eluent. The desired product was isolated as a white crystalline solid with the same physical and spectroscopic characteristics as d4U produced by an alternative method. M.p. 155° C. 1H NMR (360 Mhz, D2O/DMSO) 7.8 (d, 1H, H6), 6.7 (m, 1H, H1'), 6.37 (m, 1H, H2'), 5.8 (m, 1H, H3'), 5.56 (d, 1H, H5), 4.7 (m, 1H, H4'), 3.6 (m, 2H, H5'). 13C NMR (70 Mhz, D2O/DMSO) 163 (C4), 151 (C2), 141 (C2'), 135 (C3'), 126 (C6), 101 (C5), 89 (C1'), 87 (C4'), 62 (C5').

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05212294
Quelldatensatzuspto-grants-1993_05
ORD IDord-7594f2a196c44593b7c5773cc7805d8c
Quellennotizuspto-grants-1993_05