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HRID 50564Erstellt: 24. Oktober 2026

Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → (E)-3-[4-(2-Pyrimidinyl)phenyl]-2-propenal

https://huagongshe.com/de/reaction/50564

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
Edukt(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromideHCID 2724194—
Edukt4-(Pyrimidin-2-yl)benzaldehydeHCID 12703722—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelPotassium CarbonateHCID 11430—
Produkt(E)-3-[4-(2-Pyrimidinyl)phenyl]-2-propenalHCID 2263087057,4%

Reaktionsschritte

A mixture of 4-(2-pyrimidinyl)-benzaldehyde (1.83 g, 9.94 mmol, prepared as described in WO 9828264), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (6.45 g, 15.02 mmol), and TDA-1 (3.20 mL, 10.00 mmol) in dichloromethane (50 mL) and sat. aq. K2CO3 (50 mL) was heated to reflux for 20 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. THF (25 mL) and 10% HCl (25 mL) were added and the mixture was stirred for 1 h at rt. The mixture was cooled to 0° C., the precipitated solids were removed by filtration, washed with water and air-dried. Recrystallization from 2-propanol provided 1.20 g (57%) of the title compound as a light yellow solid. MS 211 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713455B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-4da97e34da684bd08056b982ffd70aea
Quellennotizuspto-grants-2004_03