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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835696Generated: October 25, 2026

Water → (R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthine

https://huagongshe.com/reaction/1835696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantParaxanthineHCID 4687—
ReactantSodium hydrideHCID 24758—
Reactant(R)-5-Acetoxy-1-bromohexaneHCID 12619445—
SolventDimethyl SulfoxideHCID 679—
Product(R)-5-Acetoxy-1-bromohexaneHCID 12619445—
Product(R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthineHCID 54338253120.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirring solution of 1,7-dimethylxanthine (0.30 g, 1.67 mmol) in dimethylsulfoxide (20 ml) was added sodium hydride (42 mmg, 1.75 mmol) in one portion. After stirring for 30 minutes, (R)-5-acetoxy-1-bromohexane (0.31 g, 1.75 mmol) was added neat. (R)-5-Acetoxy-1-bromohexane was prepared according to methods described in U.S. patent application Ser. No. 09/002,345, which is incorporated herein by reference. After heating at 80° C. for 18 hours, water (25 ml) was added and the aqueous solution was extracted with dichloromethane (3×20 ml). The combined extracts were washed with saturated aqueous sodium chloride solution (50 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)-3-(5-acetoxyhexyl)-1,7-dimethylxanthine (0.34 g, 64% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774130B2
Source datasetuspto-grants-2004_08
ORD IDord-38e733cee3844851a04ddd5dfa6c63b5
Source noteuspto-grants-2004_08