HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986086Generated: November 1, 2026
2-Fluoronicotinic acid → HCID 57721337, compound
https://huagongshe.com/reaction/1986086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoronicotinic acid | HCID 96089 | — |
| Reactant | HCID 57721334 | HCID 57721334 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 57721337 | HCID 57721337 | 76.1% |
Reaction Steps
A mixture of 2-fluoronicotinic acid (Aldrich, 0.42 g, 2.9 mmol) in thionyl chloride (15 mL) was refluxed for two hours before being concentrated in vacuo to a residue which was used without further purification. The residue was dissolved in anhydrous DCM (5 mL) then added dropwise to a 0° C. solution of 2-(2-(tert-butyldiphenylsilyloxy)ethyl)aniline (1.10 g, 2.9 mmol) and TEA (0.43 mL, 3.1 mmol) in anhydrous DCM (15 mL). The reaction was then stirred at ambient temperature for 16 hours before being quenched with water then stirred for an additional thirty minutes. The layers were separated and the aqueous layer extracted with DCM. The combined organic layers were washed sequentially with water, saturated aqueous NaHCO3, and brine before being dried over anhydrous MgSO4, and then concentrated in vacuo. The resultant residue was purified by silica gel flash chromatography, eluting with 4:1 hexane/EtOAc, to afford the desired compound as a white solid (1.1 g, 72%). 1H NMR (DMSO-d6) δ 9.93 (s, 1H), 8.41 (d, 1H, J=4.4 Hz), 8.22 (t, 1H, J=7.6 Hz), 7.27-7.60 (m, 15H), 3.84 (t, 2H, J=6.7 Hz), 2.98 (t, 2H, J=6.7 Hz), 0.92 (s, 9H); HRMS(ESI+), 499.2217 (M+H)+ calc, 499.2230 (M+H)+ found.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07547782B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-ba73c5755ba547838ba8a63861d27f78 |
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| Source note | uspto-grants-2009_06 |
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