Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Chloro-1-hexanol | HCID 74828 | — |
| Reactant | 6-Hydroxy-2-naphthoic acid | HCID 85557 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22167614 | HCID 22167614 | 56.5% |
Reaction Steps
To a stirred mixture of 25.00 g (133 mmol) of 6-hydroxy-2-naphthoic acid, 2.21 g (13 mmol) of potassium iodide, 4.28 g (13 mmol) of tetrabutylammonium bromide, and 77 g of ethanol, was added dropwise 18.63 g (332 mmol) of potassium hydroxide dissolved in 38 g of water. The mixture was heated to 60° C., 19.07 g (146 mmol) of 6-chloro-1-hexanol was added dropwise here, and the solution was refluxed for 34 hours. After adding hydrochloric acid dropwise, the reaction mixture was chilled with ice-water, and the precipitate was collected by filtration. Water was added to the precipitate, and the mixture was stirred for 30 minutes and filtered to recover the precipitate, which was dried in an oven at 40° C. overnight. The dried product was recrystallized from THF to yield the desired product, 6-(6-hydroxy-hexa-1-yloxy)-2-naphthoic acid as white solid (21.63 g, Yield: 56.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683203B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-d7f5a13f95f04fdab757217cbc84bded |
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| Source note | uspto-grants-2010_03 |
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