HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740436Generated: October 31, 2026
Water → 3-(4-Pyridyloxy)-benzaldehyde dimethyl acetal
https://huagongshe.com/reaction/1740436
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Phenol, 3-(dimethoxymethyl)- | HCID 11275229 | — |
| Reactant | 4-Chloropyridinium hydrochloride | HCID 22117864 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Pyridyloxy)-benzaldehyde dimethyl acetal | HCID 22117873 | — |
Reaction Steps
A solution of 1 g of 3-hydroxybenzaldehyde dimethyl acetal and 2 g of potassium tert.butoxide in 10 ml of anhydrous dimethylformamide was heated at 60° C. under an atmosphere of dry nitrogen for 1 hour. The mixture was then cooled to room temperature and 900 mg of 4-chloropyridinium hydrochloride were added portionwise over a period of 20 minutes. The mixture was then heated at 160° C. for 18 hours, cooled, 100 ml of water were added and the product was extracted with ethyl acetate. The combined extracts were washed with 1M aqueous sodium hydroxide solution and with brine, and then dried over anhydrous magnesium sulphate. Evaporation to dryness left a brown oil which was purified by column chromatography on silica gel using hexane/ethyl acetate (gradient: 90:10 to 20:80) for the elution to give 3-(4-pyridyloxy)-benzaldehyde dimethyl acetal as a light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05969139 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-d1ac9ec4a5f641e2bed901653300194d |
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| Source note | uspto-grants-1999_10 |
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