HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258Generated: October 24, 2026
4-Fluoro-N-methylaniline → [2-(4-fluoro-N-methylanilino)-4-pyridinyl]methanol
https://huagongshe.com/en/reaction/258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluoro-N-methylaniline | HCID 68024 | — |
| Reactant | (2-Chloropyridin-4-yl)methanol | HCID 7062237 | — |
| Reagent | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | [2-(4-fluoro-N-methylanilino)-4-pyridinyl]methanol | HCID 61969960 | 0% |
Reaction Steps
In a 50 mL round-bottomed flask (t=g) was (2-chloropyridin-4-yl)methanol (.1 g, 0.70 mmol), Pd2dba3 (0.032 g, 0.03 mmol), and biphenyl-2-yldicyclohexylphosphine (0.024 g, 0.07 mmol) in toluene (6 mL) to give a dark red solution. 4-fluoro-N-methylaniline (0.096 g, 0.77 mmol) and KOtBu (.323 g, 2.88 mmol) were added. Mixture was degassed by bubbling N2 for 20 minutes, then placed in oil bath at 105 °C. Reaction went for 3 hours, at which point LC/MS was taken. No product was observed.
Provenance & Evidence
| Source dataset | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-eb19acfe7f704eb2aa769ff5f1767708 |
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| Source note | 750 AstraZeneca ELN dataset |
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