Reaktion #340594

ord-90a3c3da34174d029438d39ac7ba4ed6

Reaktionsgleichung

CC(C)OC(=O)N=NC(=O)OC(C)C
diisopropyl azodicarboxylate
COc1cc(C=O)ccc1O
4-Hydroxy-3-methoxybenzaldehyde
COc1cc(C=O)ccc1O
4-hydroxy-3-methoxybenzaldehyde
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
OCCc1ccc(Cl)cc1
4-Chlorophenylmethylcarbinol
OCCc1ccc(Cl)cc1
4-chlorophenylmethylcarbinol
COc1cc(C=O)ccc1OC(C)c1ccc(Cl)cc1
desired compound
COc1cc(C=O)ccc1OC(C)c1ccc(Cl)cc1
4-[1-(4-chloro-phenyl)-ethoxy]-3-methoxy-benzaldehyde

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigepurified by silica gel chromatography, ethyl acetate

Vorschrift

4-Chlorophenylmethylcarbinol (76, 0.668 mL, 6.57 mmol) was dissolved in tetrahydrofuran (60.0 mL) at 0° C. under an atmosphere of nitrogen. 4-Hydroxy-3-methoxybenzaldehyde (21, 1.00 g, 6.57 mmol) and triphenylphosphine (2.07 g, 7.89 mmol) were added to the reaction, followed by diisopropyl azodicarboxylate (1.55 mL, 7.89 mmol) over 10 minutes. The reaction was stirred for 2 hours. The mixture was adsorbed onto silica and purified by silica gel chromatography, ethyl acetate:hexanes, to provide the desired compound, (77, 1.14 g, 60%). 1H-NMR was consistent with the desired compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07872018B2uspto-grants-2011_01