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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Reactant | Phenol, 3-(dimethoxymethyl)- | HCID 11275229 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2-Pyrimidinyloxy)-benzaldehyde dimethyl acetal | HCID 22117859 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06162918 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-c7881455954043e4b313c398881f8d46 |
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| Source note | uspto-grants-2000_12 |
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