HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607338Generated: October 26, 2026
Sodium Iodide → 2'-deoxy-3'-O-benzyl-5'-O-trityl-5-fluorouridine
https://huagongshe.com/reaction/1607338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2'-deoxy-5'-O-trityl-5-fluorouridine | HCID 10838704 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2'-deoxy-3'-O-benzyl-5'-O-trityl-5-fluorouridine | HCID 10674723 | 70.6% |
Reaction Steps
A 10 g quantity of 2'-deoxy-5'-O-trityl-5-fluorouridine was dissolved in 100 ml of dioxane. To the solution were added 2.9 ml of benzyl chloride, 6.9 g of particles of potassium hydroxide and 3.56 g of sodium iodide. The mixture was stirred at 40° C. for 4 hours, and 2.9 ml of benzyl chloride and 1.15 g of potassium hydroxide were added and stirred for 1 hour. Thereto was added water to dissolve the potassium hydroxide in water. The solution was adjusted to a pH of about 3 with acetic acid and extracted with ethylene dichloride. The extract was washed with water and the ethylene dichloride layer was dried over anhydrous sodium sulfate. The sodium sulfate was separated by filtration and the solvent was distilled off, giving 8 g of 2'-deoxy-3'-O-benzyl-5'-O-trityl-5-fluorouridine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04864021 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-6fafbd2859c24a9ba64522945df2dff8 |
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| Source note | uspto-grants-1989_09 |
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