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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654552Generated: October 30, 2026

4-Hydroxybenzaldehyde → 4-(6-Hydroxyhexoxy)benzaldehyde

https://huagongshe.com/reaction/1654552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-1-hexanolHCID 74828—
SolventWaterHCID 962—
Product4-(6-Hydroxyhexoxy)benzaldehydeHCID 15051082—

Reaction Conditions

Temperature100 °C

Reaction Steps

2.44 g (0.02 mol) of 4-hydroxybenzaldehyde, 2.73 g (0.02 mol) of 6-chlorohexanol, 1.66 g (0.012 mol) of potassium carbonate and 20 ml of N,N-dimethylformamide were put in a three-neck 50 ml-flask equipped with a stirrer and a thermometer and heated at 100° C. for 2 hours with stirring. The reaction mixture was cooled to room temperature, poured into water containing ice and extracted with ethyl acetate. The resulting extract was dried with anhydrous sodium sulfate, and ethyl acetate was removed therefrom by distillation. The oily residue was allowed to stand at room temperature, whereupon it gradually crystallized. By silica gel thin layer chromatography (using a developer of ethyl acetate), the purity of the crystals was high. The yield of the product was 4.4 g (99.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05408009
Source datasetuspto-grants-1995_04
ORD IDord-bae6eb3f9ee34a86b3740ed70cb32abd
Source noteuspto-grants-1995_04