HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473699Generated: October 30, 2026
2-Fluoropyridine → HCID 59373935, compound
https://huagongshe.com/reaction/473699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoropyridine | HCID 9746 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Phenol, 4-amino-2-fluoro- | HCID 2735918 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59373935 | HCID 59373935 | — |
Reaction Steps
To 4-amino-2-fluorophenol (0.983 g, 7.73 mmol) was added NMP (3 mL) and 2-fluoropyridine (0.670 mL, 7.78 mmol). The reaction mixture was heated to 120° C. for 12.5 h and the temperature was increased to 150° C. After 9 h, the reaction mixture was diluted with EtOAc and the organic phase was washed with saturated NaHCO3 (1×), brine (1×), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel (10% to 70% EtOAc in hexanes) gave 2-fluoro-4-(pyridin-2-ylamino)phenol as a pale yellow oil. MS (ESI, pos. ion) m/z: 205.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637500B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-16e84d64c15a46a786cd396e4a90acd0 |
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| Source note | uspto-grants-2014_01 |
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