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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1871898Erstellt: 26. Oktober 2026

3-Pyridinecarboxaldehyde → Pyridine, 3-(2,2-dibromoethenyl)-

https://huagongshe.com/reaction/1871898

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-PyridinecarboxaldehydeHCID 10371—
EduktCarbon tetrabromideHCID 11205—
EduktTriphenylphosphineHCID 11776—
LösungsmittelDichloromethaneHCID 6344—
ProduktPyridine, 3-(2,2-dibromoethenyl)-HCID 1133452670%

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 3carboxaldehyde (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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06107298
Quelldatensatzuspto-grants-2000_08
ORD IDord-585149f9d4b94eebbc0abcc0915240e4
Quellennotizuspto-grants-2000_08