Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179671Generated: October 27, 2026

Dimethylformamide → 2-(p-Methoxyphenoxy)-3-(dimethylamino)acrolein

https://huagongshe.com/reaction/1179671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1-(2,2-Diethoxyethoxy)-4-methoxybenzeneHCID 251315—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
Product2-(p-Methoxyphenoxy)-3-(dimethylamino)acroleinHCID 5449802444%

Reaction Conditions

Temperature50 °C

Reaction Steps

Phosphorus oxychloride (18.4 g, 120 mmol) was added to dimethylformamide (8.8 g, 120 mmol), maintaining the temperature below 25° C. by an external ice-bath. Upon completion of the addition the reaction mixture was heated to 50° C. for 45 minutes and then cooled to room temperature. Chloroform (35 ml) was added and the resulting solution was brought to reflux. 4-Methoxyphenoxyacetaldehyde diethylacetal (9.61 g, 40.0 mmol) was added in portions. After heating for 3 hours at reflux the solution was cooled to room temperature and poured carefully onto a solution of potassium carbonate (115 g) in water (100 ml). The mixture was cooled in an ice-bath to around room temperature and extracted twice with dichloromethane. The combined organic layers were dried over sodium sulphate, filtered and evaporated in vacuo yielding a brown oil. The residue was heated with ethyl acetate:heptane and decanted, leaving a brown oil. The solvent was removed in vacuo to give a brown oil, which was purified by flash column chromatography (SiO2, ethyl acetate) yielding the title compound (3.87 g, 44% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279470B2
Source datasetuspto-grants-2007_10
ORD IDord-4e06b60a2f374fd4a084663af8b0537a
Source noteuspto-grants-2007_10