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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392612Generated: October 30, 2026

Acetic Acid → 1-(8-Acetoxy-9-bromononyl)-3,7-dimethylxanthine

https://huagongshe.com/reaction/2392612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(8,9-Dihydroxynonyl)-3,7-dimethylxanthineHCID 9840808—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(8-Acetoxy-9-bromononyl)-3,7-dimethylxanthineHCID 1533859796%

Reaction Steps

A mixture of 1-(8,9-dihydroxynonyl)-3,7-dimethylxanthine (428 mg, 1.3 mmol) and 30% hydrogen bromide in acetic acid (0.8 ml, 3.9 mmol) was stirred for 90 minutes. The solution was poured into a mixture of water (10 ml), sodium bicarbonate (1.35 g), and dichloromethane (10 ml). After 10 minutes of vigorous stirring the layers were separated and the aqueous portion was extracted with dichloromethane (3×15 ml). The combined organic phases were dried over sodium sulfate and the solvent was evaporated under vacuum to give 1(8-acetoxy-9-bromononyl)-3,7-dimethylxanthine (550 mg, 96% yield) as a yellow oil. Without further purification, the oil was dissolved in methanol (5 ml) and then a 1M solution of sodium methoxide in methanol (1.4 ml) was added. After 30 minutes the reaction mixture was poured into water (30 ml) and extracted with dichloromethane (3×40 ml). The combined organic phases were dried over sodium sulfate and the solvents evaporated under vacuum. The solid residue was recrystallized (dichloromethane-petroleum ether) to give 1-(8,9-oxidononyl)-3,7-dimethylxanthine (380 mg, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05801181
Source datasetuspto-grants-1998_09
ORD IDord-d0266098f99f4ea3a8df23f97d2afffe
Source noteuspto-grants-1998_09