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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154523Generated: October 30, 2026

Triethylamine → 2'-deoxy-3',5'-di-O-acetyl-5-fluoro-3-(2-methylbenzoyl)uridine

https://huagongshe.com/reaction/1154523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methylbenzoyl chlorideHCID 70276—
Reactant3',5'-Di-O-acetyl-2'-deoxy-5-fluorouridineHCID 12790164—
Solvent1,4-DioxaneHCID 31275—
Product2'-deoxy-3',5'-di-O-acetyl-5-fluoro-3-(2-methylbenzoyl)uridineHCID 13189896—

Reaction Steps

10.0 g of 2'-deoxy-3',5'-di-O-acetyl-5-fluorouridine and 10 ml of triethylamine were dissolved in 50 ml of dioxane, and the resulting mixture was cooled with ice. To the mixture was added 7.0 g of 2-methylbenzoyl chloride, and the resulting mixture was allowed to stand at room temperature for 30 minutes and then at 45° C. for 60 minutes. The crystals formed were filtered off, and the filtrate was concentrated under reduced pressure. The thus obtained oily residue was dissolved in 50 ml of ethanol by application of heat. After being cooled, the solution was inoculated, and there was obtained 2'-deoxy-3',5'-di-O-acetyl-5-fluoro-3-(2-methylbenzoyl)-uridine) as crystals. Recrystallization of the product from ethanol afforded 11.3% (yield: 84.0%) of colorless prismatic crystals having a melting point of 108° to 109° C. The structure of the product was supported by the absorption spectra and elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490366
Source datasetuspto-grants-1984_12
ORD IDord-3d01275e301b4d9583f4ed45f1d0cc83
Source noteuspto-grants-1984_12