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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275834Generated: November 1, 2026

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

https://huagongshe.com/reaction/1275834

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 numberUS06162918
Source datasetuspto-grants-2000_12
ORD IDord-c7881455954043e4b313c398881f8d46
Source noteuspto-grants-2000_12