HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190786Generated: October 31, 2026
2-Methoxyethanol → 2-[3-(2-Methoxyethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazole
https://huagongshe.com/reaction/2190786
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxyethanol | HCID 8019 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(3-Fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazole | HCID 66880180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[3-(2-Methoxyethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazole | HCID 66880622 | — |
Reaction Steps
A mixture of 0.28 g of 2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzoxazole, 0.27 g of potassium carbonate and 3 ml of 2-methoxyethanol was stirred while heating at 80° C. for 2.5 hours. The reaction mixture was cooled to room temperature, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.23 g of 2-[3-(2-methoxyethoxy)pyridin-4-yl]-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 120”).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324387B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-c16f2f7b0748422f92a0cc07b19fadfc |
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| Source note | uspto-grants-2012_12 |
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