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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252477Generated: October 31, 2026

Sodium Iodide → Methyl 8-(dodecyloxy)quinoline-2-carboxylate

https://huagongshe.com/reaction/252477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-BromododecaneHCID 8919—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 8-Hydroxyquinoline-2-CarboxylateHCID 12336161—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 8-(dodecyloxy)quinoline-2-carboxylateHCID 6687245414%

Reaction Steps

In a first step, dodecyl bromide (767 μL, 3.2 mmol), NaI (478 mg, 3.2 mmol) and NaH (76 mg, 3.2 mmol) were added to a solution of 8-hydroxyl-quinoline-2-carboxylic acid methyl ester (2.11 mmol) stirring in DMF (dry, 10 mL), and the red reaction was allowed to stir overnight. The crude material resulting from removal of solvents by rotary evaporation was taken into DCM, washed with water, dried over Na2SO4, and filtered. The resulting solution was evaporated to dryness and the desired intermediate, 8-dodecyloxy-quinoline-2-carboxylic acid methyl ester, was obtained by HPLC (isocratic, 75% acetonitrile, 25% water) yielding 169 mg (about 14% yield). This intermediate was in turn deprotected using LiOH in THF/H2O as described in the method of Example 336 to yield the title compound, which was utilized further without additional purification or characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868135B2
Source datasetuspto-grants-2011_01
ORD IDord-ebd5ed555b5d43279656f61d7c912a24
Source noteuspto-grants-2011_01