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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092955Generated: October 31, 2026

4-Hydroxybenzaldehyde → p-(Hexyloxy)benzaldehyde

https://huagongshe.com/reaction/2092955

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 drying at 80° C. under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440843B2
Source datasetuspto-grants-2013_05
ORD IDord-3a267a34a0e2465c8278b4180211cbcc
Source noteuspto-grants-2013_05