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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395288Generated: October 25, 2026

Acetic Acid → 2'-Deoxy-5-iodouridine 3',5'-diacetate

https://huagongshe.com/reaction/395288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantIdoxuridineHCID 5905—
ReactantAcetic AnhydrideHCID 7918—
SolventDiethyl EtherHCID 3283—
Product2'-Deoxy-5-iodouridine 3',5'-diacetateHCID 2724347102.8%

Reaction Steps

To 5-iodo-2′-deoxyuridine (2.1) (70.8 g, 200 mmol, 1 eq) in an 500 mL Erlenmeyer flask was added acetic acid (72 g, 68.7 mL, 1200 mmol, 6 eq) and acetic anhydride (51 g, 47.1 mL, 500 mmol, 2.5 eq). In a test tube at 0° C., the catalyst for the reaction was prepared by adding HClO4 (0.5 mL) over acetic anhydride (2 mL). Five drops of the catalyst were added into the Erlenmeyer flask at 0° C. with stirring. The reaction mixture was brought to room temperature and stirred for 4 hours where upon a thick white precipitate formed. The Erlenmeyer flask was filled with ether and stirred vigorously for 30 minutes. The white precipitate was filtered and the white cake was washed with ether (500 mL). The product was dried in the vacuum oven overnight to afford (2.2) (90.1 g, 95%) 1H-NMR (CDCl3) δ(ppm) 9.40 (bs, 1 H, exchangeable, NH), 7.78 (s, 1 H, H-6), 6.18 (dd, J=8.10 Hz, 1 H, H-1′), 5.05 (m, 1 H, H-3′), 4.07-4.25 (m, 3 H, H-6), 4′, 5′), 2.35 (m, 1 H, H-2′b), 1.85-2.12 (m, 7 H, 2×CH3, H-2′a)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605611B2
Source datasetuspto-grants-2003_08
ORD IDord-f68a6e947b494bb7a61a3e0a8858c397
Source noteuspto-grants-2003_08