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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092956Generated: October 31, 2026

Water → 1-(Hexyloxy)naphthalene

https://huagongshe.com/reaction/2092956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-NaphtholHCID 7005—
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodohexaneHCID 12527—
SolventAcetonitrileHCID 6342—
Product1-(Hexyloxy)naphthaleneHCID 301720998.4%

Reaction Steps

1-naphthol (5 g, 34.7 mmol), iodohexane (8.82 g, 41.6 mmol) and K2CO3 (7.2 g, 50 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 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 7.8 g (98%) of compound 2 as an orange 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-2dceff3044464c4fad3a7f776024df2e
Source noteuspto-grants-2013_05