HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254261Generated: October 30, 2026
HCID 11172502, compound → 4-(Methoxymethoxy)benzaldehyde
https://huagongshe.com/reaction/2254261
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 11172502 | HCID 11172502 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Methoxymethoxy)benzaldehyde | HCID 250074 | 91.7% |
Reaction Steps
In 50 ml of ethanol were dissolved 6.31 g of the 2',4'-bis(methoxymethoxy)acetophenone obtained in Production Example 10 and 4.00 g of the p-methoxymethoxybenzaldehyde obtained in Production Example 25, and the solution was cooled to 0° C. and 30 ml of a saturated solution of potassium hydroxide in ethanol was added to the solution. The temperature of the reaction liquid was elevated to room temperature and the liquid was stirred for 2 days. The reaction liquid was diluted with water, neutralized with 6 N hydrochloric acid and extracted with ethyl acetate, and the organic layer was dried with sodium sulfate and concentrated under reduced pressure to obtain a reaction mixture in the form of a syrup. The syrup was subjected to the column chromatography (320 g of 270-400 mesh Kieselgel 60; 0.5 kg/cm2 ; eluting solvent: hexane/ethyl acetate=1/1). Fractions of 50 ml were collected and the 66th to 87th fractions were combined to obtain 5.64 g (yield= 55.9%) of 2',4,4'-tris(methoxymethoxy)chalcone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234951 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-b0c34ea67d5643a5a8cf19c5701cdbf7 |
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| Source note | uspto-grants-1993_08 |
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