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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 9-Pivaloyloxymethyl-3,7-dimethyluric acid | HCID 22499038 | — |
| Reactant | (R)-5-acetoxy-1-iodohexane | HCID 54009360 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (R)-1-(5-acetoxyhexyl)-9-pivaloyloxymethyl-3,7-dimethyluric acid | HCID 53725271 | 94% |
| Product | (R)-5-acetoxy-1-iodohexane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06774130B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-962dfb75bbdf4b6c8e57c4259024b174 |
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| Source note | uspto-grants-2004_08 |
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