HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555853Generated: October 27, 2026
Carbon Dioxide → 4-(3-Fluoropyrazin-2-YL)tetrahydro-2H-pyran-4-OL
https://huagongshe.com/reaction/555853
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | Tetrahydro-4H-pyran-4-one | HCID 121599 | — |
| Reactant | 2-Fluoropyrazine | HCID 642835 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(3-Fluoropyrazin-2-YL)tetrahydro-2H-pyran-4-OL | HCID 59351230 | — |
Reaction Steps
A 2.5M solution of nbuli (4.49 mL, 11.22 mmol)/hexane in THF (3 mL) was first cooled to −78° C. To the cooled solution was added dropwise, 2,2,6,6-tetramethylpiperidine (2.065 mL, 12.24 mmol). The dry ice bath was then switched to a 0° C. bath. The reaction mixture was stirred for 10 min at 0° C. and then the dry ice bath was switched back to recool the reaction mixture to −78° C. To the cooled solution was added 2-fluoropyrazine (1 g, 10.20 mmol), dropwise. After 5 min of stirring at −78° C., a solution of dihydro-2H-pyran-4(3H)-one (0.937 mL, 10.20 mmol) in 0.6 mL of THF was added dropwise. The resulting mixture was allowed to gradually warm to room temperature overnight. Reaction was quenched with saturated NH4Cl and extracted with EtOAc. Purification by Biotage (0-100% EtOAc/hexane) produced product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053438B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-159c35b1176f47b795e16e9f409273dc |
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| Source note | uspto-grants-2011_11 |
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