HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1760Erstellt: 23. Oktober 2026
3-Pyridinecarboxaldehyde → Pyridine, 3-(2,2-dibromoethenyl)-
https://huagongshe.com/de/reaction/1760
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Edukt | Carbon tetrabromide | HCID 11205 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Pyridine, 3-(2,2-dibromoethenyl)- | HCID 11334526 | 70% |
Reaktionsschritte
Tetrabromomethane (24.82 g, 0.747 mole) and triphenylphosphine (39.17 g, 0.149 mole) were stirred together in dry methylene chloride (100 mL) for 5 min. at 0° C. under a nitrogen atmosphere. To this mixture was added dropwise pyridine 3-carboxaldehyde (4 g, 0.0373 mole). The solution was then stirred for 45 min. at ambient temperature. The reaction mixture was extracted with aqueous 6N hydrochloric acid (3×25 mL), the aqueous layer basified with solid sodium bicarbonate to pH 8-9 and extracted with chloroform (4×25 mL). The combined organic liquours were dried over anhydrous sodium sulfate, filtered and concentrated on a rotary evaporator to give a dark colored syrup. The crude product was chromatographed on silica gel (70-230 mesh) with chloroform:methanol (95:5) as eluant, to afford a light yellow solid (5.0 g, 70%) which rapidly turned dark on standing.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05726316 |
|---|
| Quelldatensatz | uspto-grants-1998_03 |
|---|
| ORD ID | ord-b463cdcceaba4202b2513724f75023cf |
|---|
| Quellennotiz | uspto-grants-1998_03 |
|---|