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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361486Generated: October 27, 2026

Carbon Dioxide → 1-(5-Acetoxy-6-bromohexyl)-3,7-dimethylxanthine

https://huagongshe.com/reaction/361486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(5,6-Dihydroxyhexyl)-3,7-dimethylxanthineHCID 15895955—
ReactantAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
Product1-(5-Acetoxy-6-bromohexyl)-3,7-dimethylxanthineHCID 2329597396%

Reaction Steps

To 1-(5,6-dihydroxyhexyl)-3,7-dimethylxanthine 1.0 g, 3.38mmol) was added 30% hydrogen bromide-acetic acid (3.4 mL) over 30 seconds and then stirred for 2.5 hours until all of the solid dissolved. The solution was poured carefully over a mixture of sodium bicarbonate (12 g) and ice water (50 mL). After carbon dioxide evolution had subsided, the mixture was extracted with dichloromethane (3×25 mL). The combined extracts were dried over magnesium sulfate and the solvent evaporated under vacuum, yielding 1.3 g (3.24 mmol, 96%) 1-(5-Acetoxy-6-bromohexyl)-3,7-dimethylxanthine as a viscous oil, dissolved in methanol (5 mL). A 1M sodium methoxide in methanol solution (3.9 mL) was added over 30 seconds. After stirring for 20 minutes, the solution was reated with water (20 mL) and then extracted with dichloromethane (3×15 mL). The combined extracts were dried over magnesium sulfate and the solvents were evaporated under vacuum to yield 900 mg (3.24 mmol, 100% yield) 1-(5,6-Oxidohexyl)-3,7-dimethylxanthine as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866576
Source datasetuspto-grants-1999_02
ORD IDord-f822b9deae4846f3ad09e1ad4e4f3161
Source noteuspto-grants-1999_02