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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462040Generated: October 25, 2026

8-Hydroxyquinoline → 7-Dodecenyl-8-hydroxyquinoline

https://huagongshe.com/reaction/462040

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantPotassium IodideHCID 4875—
ReactantSodium HydroxideHCID 14798—
Reactant1-Chlorododec-1-eneHCID 122939—
SolventMethanolHCID 887—
Product7-Dodecenyl-8-hydroxyquinolineHCID 53761966—

Reaction Conditions

Temperature230 °C

Reaction Steps

One hundred forty five grams (1.0 mole) 8-hydroxyquinoline, 40 gm. sodium hydroxide, 500 ml. methanol and 5 gm. potassium iodide were combined in a two liter round bottom flask. To this was added 243 gm. dodecenyl chloride (as used in Example I) and the mixture stirred under reflux overnight. The product was filtered, taken up in ether and washed with 500 ml. Claisen's alkali (in five portions). The ether solution was washed several times with water until neutral, dried and the solvent stripped to yield 317.9 gm. of crude product. Of this amount, 310.9 gm. was distilled through a one foot Vigreaux after being heated in the pot to 230° C. and cooled to about 100° C. The fractions coming off at 197°-202° C., 0.7 mm. Hg. (51.1 gm.) and 202°-231° C., 0.8 mm. Hg. (96.8 gm.) consisted almost entirely of 7-dodecenyl-8-hydroxyquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04065455
Source datasetuspto-grants-1977_12
ORD IDord-dfb092fbf22c43169828ac05181c1d4a
Source noteuspto-grants-1977_12