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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1-Bromododecane | HCID 8919 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 8-Hydroxyquinoline-2-Carboxylate | HCID 12336161 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 8-(dodecyloxy)quinoline-2-carboxylate | HCID 66872454 | 14% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868135B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-ebd5ed555b5d43279656f61d7c912a24 |
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| Source note | uspto-grants-2011_01 |
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