HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062066Generated: October 26, 2026
Potassium Iodide → 1-(6-Chloro-pyridin-3-ylmethoxy)-naphthalene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/2062066
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2,4,6-Tris((dimethylamino)methyl)phenol | HCID 7026 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Naphthalenecarboxylic acid, 1-hydroxy-, methyl ester | HCID 70358 | — |
| Reactant | 2-Chloro-5-(chloromethyl)pyridine | HCID 155479 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(6-Chloro-pyridin-3-ylmethoxy)-naphthalene-2-carboxylic acid methyl ester | HCID 86619674 | 99.9% |
Reaction Steps
To a solution of 1.0 g 1-hydroxy-2-naphthoic acid methyl ester in 20 ml abs. DMF 3.22 g cesium carbonate was added, followed by addition of 0.16 g potassium iodide and 0.96 g 2-chloro-5-chloromethyl-pyridine. Under argon-atmosphere the reaction mixture was heated to 60° C. for 1 h. The mixture was then poured into water and extracted with ethyl acetate at pH9 three times. The combined organic layers were dried over magnesium sulphate, filtrated and after removal of the solvent a crude product was obtained which was recrystallized from diethyl ether to yield 1.62 g 1-(6-chloro-pyridin-3-ylmethoxy)-naphthalene-2-carboxylic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283479B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-33fe749da4b24e059f4e1b5fa4b0c7ba |
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| Source note | uspto-grants-2012_10 |
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