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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259170Generated: November 2, 2026

Sodium Chloride → 2',3'-di-O-acetyl-5'-deoxy-5-fluorocytidine

https://huagongshe.com/reaction/2259170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
Reactantbeta-D-Ribofuranose, 5-deoxy-, 1,2,3-triacetateHCID 11821332—
ReactantHCID 178509021HCID 178509021—
SolventAcetonitrileHCID 6342—
Product2',3'-di-O-acetyl-5'-deoxy-5-fluorocytidineHCID 1180963549%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium iodide (3.6 g) and chlorotrimethylsilane (794 ml) in dry acetonitrile (15 ml) was stirred with molecular sieves 4A (200 mg) at 0° C. for 5 minutes (colorless sodium chloride deposited during stirring). 1,2,3-Tri-O-acetyl-5-deoxy-β-D-ribofuranose (2.0 g) was added and the mixture was stirred at 0° C. for 30 min. Then, a solution of the trimethylsilylated 5-fluorocytosine, freshly prepared from 5-fluorocytosine (1.12 g), in dry acetonitrile (5 ml) was added at 0° C. and stirring was continued for 3 h at room temperature. The mixture was filtered, the filtrate was concentrated in vacuo, and the residue was partitioned between dichloromethane and saturated aq. sodium bicarbonate solution. The aqueous layer was extracted with CH2Cl2 /MeOH (10:1). The combined organic layers were dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was purified by silica gel chromatography using CH2Cl2 /MeOH (15:1) as an eluent, followed by recrystallization from isopropanol to give 1.24 g of 2',3'-di-O-acetyl-5'-deoxy-5-fluorocytidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05472949
Source datasetuspto-grants-1995_12
ORD IDord-91c99bf71296480490750b5424984162
Source noteuspto-grants-1995_12