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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356612생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/356612

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrogen BromideHCID 260—
반응물Sodium BicarbonateHCID 516892—
반응물1-(8,9-Dihydroxynonyl)-3,7-dimethylxanthineHCID 9840808—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물1-(8-Acetoxy-9-bromononyl)-3,7-dimethylxanthineHCID 1533859796%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05837703
출처 데이터셋uspto-grants-1998_11
ORD IDord-5fa59b946fee4b1091d66360848537b1
출처 메모uspto-grants-1998_11