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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729239Generated: October 27, 2026

Toluene → Uridine pyruvate

https://huagongshe.com/reaction/729239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantUridineHCID 6029—
Reactant2-Oxopropanoyl chlorideHCID 521791—
ReactantDichloromethane methanolHCID 21226129—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
ProductUridine pyruvateHCID 9879851—

Reaction Steps

Uridine (3.0 g, 12 mmol) was dried by toluene azeotrope under vacuum (3×), and then dissolved in DMF (20 mL) and pyridine (20 mL). The resultant solution was cooled to −10 degrees C. and 6.0 mL of pyruvyl chloride (produced in step A above) was added dropwise. The reaction mixture was stirred at room temperature under argon for 24 hours. Analysis by TLC (5% MeOH/CH2Cl2) showed the consumption of uridine. The reaction mixture was evaporated to dryness and partitioned between CH2Cl2 and aqueous sodium bicarbonate. The organic layer was washed with water, aqueous HCl (pH 3.0), and water; dried over sodium sulfate; concentrated; and purified using flash chromatography (silica gel, 5% MeOH/C2Cl2) to yield 1.4 g of uridine pyruvate, or 2′,3′,5′-tri-O-pyruvyluridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582619B2
Source datasetuspto-grants-2009_09
ORD IDord-5cb8952656394950ae7fa05c149d5a6a
Source noteuspto-grants-2009_09