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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703525Generated: October 31, 2026

4-Hydroxybenzaldehyde → p-(2-(Dimethylamino)ethoxy)benzaldehyde

https://huagongshe.com/reaction/703525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
Reactant2-Chloro-N,N-dimethylethylamineHCID 7901—
ReactantDiisopropyl EtherHCID 7914—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productp-(2-(Dimethylamino)ethoxy)benzaldehydeHCID 8482371.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 61.1 g of p-hydroxybenzaldehyde in 240 ml of N,N-dimethylformamide was added 138 g of potassium carbonate, 80.7 g of 2-dimethylaminoethyl chloride and 30 ml of isopropyl ether. The mixture was stirred at 60° C. for 1.5 hours. After cooling, the reaction mixture was poured into 720 ml of water, and the whole was extracted with chloroform. The chloroform layer was extracted with aqueous hydrochloric acid. The aqueous layer was made alkaline with aqueous sodium hydroxide solution and extracted with ethyl acetate. The extract was washed with water, dried and evaporated. The residue was distilled to give 69.1 g of colorless oil, b.p. 142°-144° C. (4 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983633
Source datasetuspto-grants-1991_01
ORD IDord-aba9b1ab47284d8baf0d2e74d53d3fa9
Source noteuspto-grants-1991_01