HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814920Generated: October 31, 2026
Sodium hydride → (R)-1-(5-acetoxyhexyl)-7-benzyl-3,8-dimethylxanthine
https://huagongshe.com/reaction/1814920
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Acetoxy-1-chlorohexane | HCID 3618051 | — |
| Reactant | 7-Benzyl-3,8-dimethylxanthine | HCID 14712608 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-Acetoxy-1-chlorohexane | HCID 3618051 | — |
| Product | (R)-1-(5-acetoxyhexyl)-7-benzyl-3,8-dimethylxanthine | HCID 54438002 | 154.8% |
Reaction Steps
7-Benzyl-3,8-dimethylxanthine (500 mg, 1.85 mmol) was added to a suspension of sodium hydride (50.5 mg) in anhydrous dimethylsulfoxide (20 ml). After stirring for 30 minutes, (R) 5-acetoxy-1-chlorohexane (357 mg) was added and the mixture was warmed to 70-80° C. for 12 hours. The (R) 5-acetoxy-1-chlorohexane was prepared according to methods described in U.S. Pat. No. 5,629,423 issued to Klein, J. P., Leigh, A. J., Michnick, J., Kumar, A. M., Underiner, G. E., on May 13, 1997. After cooling to room temperature, the reaction wash quenched by the addition of water (50 ml) and extracted with ethyl acetate (3×75 ml). The combined extracts were washed with water (2×50 ml), washed with saturated aqueous sodium chloride solution (50 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate to give (R)-1-(5-acetoxyhexyl)-7-benzyl-3,8-dimethylxanthine (638 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878715B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-2b4412f1222849f29f3b211935407cc9 |
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| Source note | uspto-grants-2005_04 |
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