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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835699Generated: October 31, 2026

Water → (R)-1-(5-acetoxyhexyl)-9-pivaloyloxymethyl-3,7-dimethyluric acid

https://huagongshe.com/reaction/1835699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant9-Pivaloyloxymethyl-3,7-dimethyluric acidHCID 22499038—
Reactant(R)-5-acetoxy-1-iodohexaneHCID 54009360—
SolventDimethyl SulfoxideHCID 679—
Product(R)-1-(5-acetoxyhexyl)-9-pivaloyloxymethyl-3,7-dimethyluric acidHCID 5372527194%
Product(R)-5-acetoxy-1-iodohexaneHCID 54009360—

Reaction Steps

To a stirring solution of 9-pivaloyloxymethyl-3,7-dimethyluric acid (0.14 g, 0.45 mmol) in dimethylsulfoxide (10 ml) was added sodium hydride (12 mg, 0.47 mmol) in one portion. The solution was stirred for 15 minutes. (R)-5-Acetoxy-1-iodohexane (0.13 g, 0.47 mmol) in dimethylsulfoxide (1 ml) was added. The solution of (R)-5-acetoxy-1-iodohexane was prepared according to methods described in U.S. patent application Ser. No. 09/002,345, which is incorporated herein by reference. After stirring at room temperature for 24 hours, water (25 ml) was added and the aqueous solution was extracted with ethyl acetate (3×15 ml). The combined extracts were washed with saturated aqueous sodium chloride solution (15 ml), dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica eluting with ethyl acetate to give (R)-1-(5-acetoxyhexyl)-9-pivaloyloxymethyl-3,7-dimethyluric acid (0.10 g, 50% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774130B2
Source datasetuspto-grants-2004_08
ORD IDord-962dfb75bbdf4b6c8e57c4259024b174
Source noteuspto-grants-2004_08