HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466088Generated: October 26, 2026
Chlorotrimethylsilane → 3'-O-benzyl-2'-deoxy-3-benzoyl-5-fluorouridine
https://huagongshe.com/reaction/466088
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzoyl bromide | HCID 12056 | — |
| Reactant | Uridine, 2'-deoxy-5-fluoro-3'-O-(phenylmethyl)- | HCID 10664574 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3'-O-benzyl-2'-deoxy-3-benzoyl-5-fluorouridine | HCID 13715061 | 54% |
Reaction Steps
To a solution of 0.50 g of 3'-O-benzyl-2'-deoxy-5-fluorouridine in 20 ml of dioxane were added 0.75 ml of trimethylchlorosilane and 2.00 ml of triethylamine, and the mixture was stirred at room temperature for 2 hours. Then, the resulting mixture was left to stand at 60° C. for 30 minutes. To the reaction mixture were added 0.42 g of benzoyl bromide and 1.00 ml of triethylamine, and the mixture was left to stand at 60° C. for 1 hour. The solvent was distilled off and the residue was dissolved in 50 ml of ethyl acetate. Then, the solution was washed with saturated aqueous solution of sodium chloride. The ethyl acetate layer was separated and concentrated. The residue was dissolved in 30 ml of methanol and 0.5 ml of acetic acid was added thereto. The mixture was left to stand overnight. The solvent was distilled off and the residue was applied to a silica gel column to conduct gradient elution using chloroform and mixtures of methanol (up to 2%) and chloroform, giving 0.35 g of the title compound as a powder in a yield of 54%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155113 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-7f7e4ddbf85541019e3aa15dd7257b95 |
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| Source note | uspto-grants-1992_10 |
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