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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740440Generated: November 1, 2026

Water → 3-(2-Pyrazinyloxy)-benzaldehyde dimethyl acetal

https://huagongshe.com/reaction/1740440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloropyrazineHCID 73277—
ReactantPhenol, 3-(dimethoxymethyl)-HCID 11275229—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product3-(2-Pyrazinyloxy)-benzaldehyde dimethyl acetalHCID 22117816—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 168 mg of 3-hydroxybenzaldehyde dimethyl acetal in 10 ml of anyhydrous dimethylformamide was stirred under nitrogen and 220 mg of potassium tert-butoxide were added. The mixture was heated at 60° C. for 1 hour, then cooled to room temperature and 115 mg of 2-chloropyrazine were added in portions. The mixture was then heated at 160° C. for 18 hours. After cooling 15 ml of water were added and the product was extracted with 50 ml of ethyl acetate. The extract was washed with 25 ml of 1M sodium hydroxide solution and 25 ml of brine and then dried over anhydrous magnesium sulphate. After filtration and evaporation of the filtrate the residual yellow oil was purified by column chromatography on silica gel using ethyl acetate/hexane (1:1) for the elution to give 3-(2-pyrazinyloxy)-benzaldehyde dimethyl acetal as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05969139
Source datasetuspto-grants-1999_10
ORD IDord-7533f8b0bc114c87a50d212b5b25431f
Source noteuspto-grants-1999_10