Reaktion #44558

ord-133c1a5c2ec548809336e842237d8715

Reaktionsgleichung

Clc1cncc(Cl)n1
2,6-dichloropyrazine
Oc1cccc(Cl)c1
3-chlorophenol
CCOC(C)=O
AcOEt
Clc1cccc(Oc2cncc(Cl)n2)c1
title compound
Ausbeute 85.0%
Clc1cccc(Oc2cncc(Cl)n2)c1
2-Chloro-6-(3-chlorophenyl-oxy)-pyrazine
Ausbeute 85.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Using Method DD with 2,6-dichloropyrazine (250 mg, 1.69 mmol) and 3-chlorophenol (193 μL, 1.86 mmol, d=1.24 g/mL), and purification by column chromatography (AcOEt:cyclohexane, 1:1), the title compound was obtained (346 mg). Yield: 85%. 1H NMR (250 MHz, DMSO-d6) δ 7.32 (dd, 1H, Harom 4, Jo=8.2 Hz, Jm=1.9 Hz), 7.43 (d, 1H, Harom 6, J=8.0 Hz), 7.50 (d, 1H, Harom 2, Jm=1.9 Hz), 7.56 (t, 1H, Harom 5, J=8.1 Hz), 8.59 (s, 1H, HPz 5), 8.62 (s, 1H, HPz 3). m/z: 241.1 [(M+H)+, calcd for C10H6Cl2N2O 240.0].

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737152B2uspto-grants-2010_06