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HRID 356612作成日:2026年10月27日

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

https://huagongshe.com/reaction/356612

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrogen BromideHCID 260—
反応物Sodium BicarbonateHCID 516892—
反応物1-(8,9-Dihydroxynonyl)-3,7-dimethylxanthineHCID 9840808—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物1-(8-Acetoxy-9-bromononyl)-3,7-dimethylxanthineHCID 1533859796%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05837703
出典データセットuspto-grants-1998_11
ORD IDord-5fa59b946fee4b1091d66360848537b1
出典メモuspto-grants-1998_11