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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386647Generated: November 1, 2026

Acetic Acid → 7-Benzyl-3-butylxanthine

https://huagongshe.com/reaction/2386647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantButyl iodideHCID 10962—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Benzyl-1H-purine-2,6(3H,7H)-dioneHCID 12500507—
SolventDimethylformamideHCID 6228—
Product7-Benzyl-3-butylxanthineHCID 399386645%

Reaction Steps

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+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268839B2
Source datasetuspto-grants-2012_09
ORD IDord-764959fe6d3443aa9a5364c5190f6423
Source noteuspto-grants-2012_09