HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842201Generated: October 30, 2026
Water → 5-(Fluoromethoxy)pyrazine-2-carboxylic acid
https://huagongshe.com/reaction/1842201
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Reactant | 2-Pyrazinecarboxylic acid, 5-(fluoromethoxy)-, methyl ester | HCID 57475677 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Fluoromethoxy)pyrazine-2-carboxylic acid | HCID 57475676 | — |
Reaction Steps
Potassium trimethylsilanolate (18.6 mg) was added to a solution of methyl 5-fluoromethoxypyrazine-2-carboxylate obtained in Preparation Example 15-(1) (18.0 mg) in tetrahydrofuran (1.0 mL). The reaction solution was stirred at room temperature for one hour. Water and ethyl acetate were added to the reaction solution, and the aqueous layer was separated. The aqueous layer was made acidic with 1 M hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure to obtain a crude product of the title compound (10.2 mg). The compound was used for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946210B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-57bae763ca00431892aebb898092ad1e |
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| Source note | uspto-grants-2015_02 |
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