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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2234962생성일: 2026년 10월 24일

Acetic Acid → 7-Benzyl-3-butylxanthine

https://huagongshe.com/ko/reaction/2234962

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Butyl iodideHCID 10962—
반응물Potassium CarbonateHCID 11430—
반응물7-Benzyl-1H-purine-2,6(3H,7H)-dioneHCID 12500507—
용매DimethylformamideHCID 6228—
생성물7-Benzyl-3-butylxanthineHCID 399386645%

반응 단계

7-benzyl-3,7-dihydro-1H-purine-2,6-dione (17.14 g, 70.8 mmol) [Synthetic Communications, 20(16), 2459-2467, 1990] and potassium carbonate (11.43 g, 82.8 mmol) were suspended in DMF (400 mL) at 40° C. After stirring for thirty minutes, butyl iodide (8.76 mL, 77.0 mmol) was added, and the mixture was stirred at 40° C. overnight. 50% Aqueous acetic acid (60 mL) was added, and the solution was concentrated under reduced pressure. The residue was suspended in water (500 mL), and the products were extracted into chloroform. The organics were collected, concentrated, and product was isolated using flash chromatography eluting with 1% methanol in dichloromethane to provide the product (9.49 g, 45%); 1H NMR (400 MHz; CDCl3) δ: 0.95 (3H, t), 1.34-1.41 (2H, m), 1.70-1.78 (2H, m), 4.05 (2H, t), 5.46 (2H, s), 7.31-7.40 (5H, m), 7.56 (1H, s), 8.21 (1H, br.s); m/z 299[MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07713982B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-c60e62b786e647abb187e6629f772184
출처 메모uspto-grants-2010_05