HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29507Erstellt: 23. Oktober 2026
Hydrochloric Acid → (2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanone
https://huagongshe.com/de/reaction/29507
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 4-Cyanopyridine | HCID 7506 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Boron Trichloride | HCID 25135 | — |
| Edukt | 3,4-Difluoroaniline | HCID 77469 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Trichloroethylene | HCID 6575 | — |
| Produkt | (2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanone | HCID 22327317 | — |
Reaktionsschritte
BCl3 (6.2 ml, 1M in DCM) was added drop wise to 1,2-difluoro-4aminobenzene (0.5 g, 0.004 mol) in trichloroethylene (6.5 ml) at 0° C. and this mixture stirred for 15 min. 4-Cyanopyridine (0.48 g, 0.005 mol) was added and the solution was warmed to RT and stirred for 30 min. The solution was then heated at 80-90° C. for 1 h. The resulting solution was refluxed at 160° C. for 4 hr and stirred at RT over night. 3N HCl was added to the reaction mixture and refluxed at 110° C. for 1.5 h. The reaction mixture was cooled to RT and made basic (pH=12) with 6N NaOH. The reaction mixture was diluted with water and DCM. The resulting two layers were separated and the aqueous layer was extracted with DCM, dried over sodium sulphate and concentrated. The compound was purified by column chromatography using silica gel to yield title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07420055B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-590fb90e5aed4c9387b4cf70831341c8 |
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| Quellennotiz | uspto-grants-2008_09 |
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