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HRID 76878Erstellt: 24. Oktober 2026

Toluene → 3-(1-Tritylimidazol-4-YL) propionaldehyde

https://huagongshe.com/de/reaction/76878

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktPotassium Sodium TartrateHCID 9357—
EduktDiisobutylaluminum hydrideHCID 14487—
EduktMethyl 3-(1-Tritylimidazol-4-yl) PropionateHCID 10475868—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(1-Tritylimidazol-4-YL) propionaldehydeHCID 11451428—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

3-(1-Trityl-1H-imidazol-4-yl)propionic acid methyl ester (7.75 g, 19.5 mmol), J. Org. Chem. 2000, 65, 2229-2230, is dissolved in DCM (300 mL) and cooled to −78° C. To this is added a toluene solution of DIBAL (21.0 mL, 1.5 M). After 2 h MeOH (20 mL) is added followed by saturated aqueous Rochelle salt solution (50 mL). The mixture is partitioned between DCM and saturated aqueous Rochelle salt solution. The organic phase is dried (Na2SO4) and evaporated. The crude residue is purified via flash column chromatography (MeOH/DCM 1:99→MeOH/DCM 5:95) to give the aldehyde, 3-(1-trityl-1H-imidazol-4-yl)propionaldehyde as a yellow gum (cas #184030-88-4). 1H NMR (CDCl3) δ 9.83 (s, 1H), 7.38-7.31 (m, 10H), 7.16-7.12 (m, 6H), 6.58 (s, 1H), 2.90 (t, J=8.0 Hz, 2H), 2.83-2.79 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835646B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-be1999ba89174bc396a9555d08f6c297
Quellennotizuspto-grants-2014_09