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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030744Generated: October 30, 2026

HCID 11172502, compound → 4-(Methoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/1030744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11172502HCID 11172502—
SolventEthanolHCID 702—
Product4-(Methoxymethoxy)benzaldehydeHCID 25007491.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106871
Source datasetuspto-grants-1992_04
ORD IDord-772e6235962e48f990747f07b40580ca
Source noteuspto-grants-1992_04