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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975232Generated: October 23, 2026

Iodine → 2',3'-Dideoxy-5-iodocytidine

https://huagongshe.com/en/reaction/975232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDideoxycytidineHCID 24066—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2',3'-Dideoxy-5-iodocytidineHCID 1463010483%

Reaction Steps

A solution of 2',3'-dideoxycytidine (2.11 g, 10 mmol, Raylo) and mercuric acetate (3.35 g, 10.5 mmol, Fisher) in 50 mL of methanol was refluxed for 19 hours. The resulting white suspension was diluted with methanol (50 mL) and dichloromethane (100 mL). Iodine (3.05 g, 12 mmol) was added and the suspension was stirred at 25°. After 4 hours, the free base form of AG3X4A resin (20 mL, 38 meq, Bio-Rad) was added and hydrogen sulfide was bubbled into the reaction for 15 minutes. Complete precipitation of mercury(II) was verified by TLC. The reaction was filtered through filter aid and the filter aid was washed with 1:1 methanol-dichloromethane. The filtrate was evaporated onto silica gel (10 g) and the loaded silica gel was placed on top of a 150 g silica gel column. Elution with 5%, 10% and 20% methanol in dichloromethane afforded 2.79 g (83%) of iodide 19 as a colorless crystalline solid. Two recrystallizations from boiling water afforded, after vacuum-drying at 50°, large, analytically-pure prisms (mp: d 178°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608063
Source datasetuspto-grants-1997_03
ORD IDord-9c730f1003874ab187e93e6615c265c2
Source noteuspto-grants-1997_03