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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740442Generated: November 4, 2026

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

https://huagongshe.com/reaction/1740442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-ChloropyrimidineHCID 74404—
ReactantPhenol, 3-(dimethoxymethyl)-HCID 11275229—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product3-(2-Pyrimidinyloxy)-benzaldehyde dimethyl acetalHCID 22117859—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 168 mg of 3-hydroxybenzaldehyde dimethyl acetal in 2 ml of anhydrous 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 114 mg of 2-chloropyrimidine were added in portions. The mixture was heated at 150° C. for 20 hours. After cooling 20 ml of water were added and the product was extracted with ethyl acetate. The extracts were washed with 10 ml of 1M sodium hydroxide solution and 5 ml of brine and then dried over anhydrous magnesium sulphate. After filtration and evaporation of the filtrate the residual brown gum was purified by column chromatography on silica gel using ethyl acetate/hexane (1:1) for the elution to give 3-(2-pyrimidinyloxy)-benzaldehyde dimethyl acetal as a syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05969139
Source datasetuspto-grants-1999_10
ORD IDord-22e4f265ca6249b79a9147b473a8377d
Source noteuspto-grants-1999_10