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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129881Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/129881

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrogen BromideHCID 260—
EduktSodium BicarbonateHCID 516892—
Edukt1-(8,9-Dihydroxynonyl)-3,7-dimethylxanthineHCID 9840808—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(8-Acetoxy-9-bromononyl)-3,7-dimethylxanthineHCID 1533859796%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05470878
Quelldatensatzuspto-grants-1995_11
ORD IDord-90e883bca33d486aaae47fda1cfacd71
Quellennotizuspto-grants-1995_11