HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728204Generated: October 31, 2026
p-Anisoyl chloride → HCID 53936791, compound
https://huagongshe.com/reaction/728204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 18646879 | HCID 18646879 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 53936791 | HCID 53936791 | 91.4% |
Reaction Steps
To a solution of 0.30 g of 5'-O-acetyl-2'-deoxy-5-fluoro-3'-O-(2-thienyl)methyluridine in 10 ml of dioxane were added 0.55 ml of triethylamine and 0.16 g of 4-methoxy-benzoyl chloride. The mixture was stirred at 80° C. for 2 hours. The solvent was distilled off and the residue was dissolved in 30 ml of ethyl acetate. The solution was washed with water. The ethyl acetate layer was dried over sodium anhydrous sulfate and concentrated. The residue was subjected to silica gel chromatography and purified by elution with chloroform, giving 0.37 g of 5'-O-acetyl-2'-deoxy-5-fluoro-3-(4-methoxybenzoyl)-3'-O-(2-thienyl)me thyluridine in a yield of 91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05047521 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-4c2a669e7f30480b8bdb0e783962982f |
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| Source note | uspto-grants-1991_09 |
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