Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 392438Erstellt: 24. Oktober 2026

Benzyltriphenylphosphonium bromide → N-(3-(2-Phenylvinyl)phenyl)-N-(ethanesulfonyl)pyrid-3-ylmethylamine

https://huagongshe.com/de/reaction/392438

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyltriphenylphosphonium bromideHCID 2734970—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
EduktN-(3-Formylphenyl)-N-(ethanesulfonyl)pyrid-3-ylmethylamineHCID 23521699—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(3-(2-Phenylvinyl)phenyl)-N-(ethanesulfonyl)pyrid-3-ylmethylamineHCID 69881230—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Benzyltriphenylphosphonium bromide (0.765 g, 1.77 mmol) was dispersed into THF (12 ml) and cooled at 0° C. To the cooled suspension was added dropwise a solution of potassium bis(trimethylsilyl)amide (0.5 M, 3.5 ml, 1.75 mmol). After stirring at 0° C. for 1 h, a solution of). N-(3-formyl-phenyl)-N-(ethylsulfonyl)pyrid-3-ylmethylamine (0.304 g, 1.0 mmol) in THF was added. The reaction mixture was stirred at ambient temperature for 2 h. Evaporation and chromatography on silica-gel eluting with toluene-EtOAc to give the title compound. 1H NMR: 8.48 (d,1H,J=3.4 Hz), 8.30 (d,1H,J=2.0 Hz), 7.65 (d,1H,J=7.8 Hz), 7.30-6.74 (m,8H), 6.60 (q,2H,J=12.2, 37.1 Hz), 4.68 (s,2H), 2.87 (q,2H,J=7.3 Hz), 1.28 (t,3H,J=7.4 Hz). MS calcd 378.1; MS (M+1) 379.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06800651B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-5f86ebaf8dca4cb699ef961509a0e398
Quellennotizuspto-grants-2004_10