Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080645Generated: November 2, 2026

4-Hydroxybenzaldehyde → p-(Hexyloxy)benzaldehyde

https://huagongshe.com/reaction/2080645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodohexaneHCID 12527—
SolventAcetonitrileHCID 6342—
Productp-(Hexyloxy)benzaldehydeHCID 7981698.1%

Reaction Steps

4-formyl-phenol (5 g, 41 mmol), iodohexane (10.5 g, 49 mmol) and K2CO3 (8.5 g, 61 mmol) in acetonitrile (150 ml) were refluxed overnight under N2. After being cooled to room temperature, water (10 ml) was added and acetonitrile was evaporated. Water (150 ml) and Et2O (150 ml) were then added. The ethereal layer was extracted and washed with water (2×100 ml), brine (100 ml), dried over MgSO4, filtered and evaporated to dryness to afford 8.3 g (98%) of compound 1 as a slightly yellow oil after during at 80° C. under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932404B2
Source datasetuspto-grants-2011_04
ORD IDord-c816bdc00e234ffc9f02fd3f86746917
Source noteuspto-grants-2011_04