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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10665Generated: October 25, 2026

Water → 2,4-Dimethoxy-5-pyrazin-2-yl-benzaldehyde

https://huagongshe.com/reaction/10665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-(5-[1,3]Dioxolan-2-yl-2,4-dimethoxy-phenyl)-pyrazineHCID 21980998—
SolventAcetoneHCID 180—
Product2,4-Dimethoxy-5-pyrazin-2-yl-benzaldehydeHCID 2198108934.7%

Reaction Steps

Ex-46D: 2-(5-[1,3]Dioxolan-2-yl-2,4-dimethoxy-phenyl)-pyrazine (1.02 g, 3.54 mmol) was dissolved in acetone and p-toluenesulfonic acid (100 mg, 0.53 mmol) and water (5 mL) were added. The solution was stirred for 3 h at room temperature, then concentrated on the rotavap. The resulting mixture was diluted with water (50 mL) and extracted with EtOAc (3×100 mL). The organic phase was washed with 25% saturated aqueous NaHCO3, dried over sodium sulfate, filtered, and concentrated. Drying gave 0.30 g of 2,4-dimethoxy-5-pyrazin-2-yl-benzaldehyde as a yellow solid (18% yield). 1H-NMR (CDCl3) δ 10.35 (s, 1H), 9.06 (d, J=2 Hz, 1H), 8.63–8.65 (m, 1H), 8.45 (d, J=2 Hz, 1H), 8.39 (s, 1H), 6.56 (s, 1H), 4.03 (s, 3H), 4.01 (s, 3H). HRMS m/z: calc. 244.0848, found 244.0853.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094801B2
Source datasetuspto-grants-2006_08
ORD IDord-d427d4fef5b1445cbb0a32b5034db457
Source noteuspto-grants-2006_08