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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174398Generated: October 30, 2026

4-Hydroxybenzaldehyde → p-(Octyloxy)benzaldehyde

https://huagongshe.com/reaction/2174398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
Reactant1-BromooctaneHCID 8140—
ReactantPotassium CarbonateHCID 11430—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Productp-(Octyloxy)benzaldehydeHCID 90358—

Reaction Steps

A mixture of 4-hydroxybenzaldehyde (10.0 g, 81.8 mmol), 1-bromooctane (15.8 mmol, 81.8 mmol), and K2CO3 (34.0 g, 0.25 mol) in DMF (150 mL) was heated to reflux for 8 hours. After cooling the reaction back down to room temperature, the reaction mixture was diluted in toluene and the organic layer was washed with 10% HCl, brine, and water. After concentrating in vacuo, the oil was purified by short silica gel plug (10% DCM in n-hexanes). Solvent was dried in vacuo to afford the 4-octyloxy benzaldehyde as a slightly colored oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061965B2
Source datasetuspto-grants-2015_06
ORD IDord-83dc8c67da0f4adc85719f586b85ce32
Source noteuspto-grants-2015_06