HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030744Generated: October 30, 2026
HCID 11172502, compound → 4-(Methoxymethoxy)benzaldehyde
https://huagongshe.com/reaction/1030744
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 6N 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). 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 | US05106871 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-772e6235962e48f990747f07b40580ca |
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| Source note | uspto-grants-1992_04 |
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