Reaktion #613577

ord-9926d4bb4fd44d6fad390b00ff72414e

Reaktionsgleichung

COc1cc(Br)ccn1
4-bromo-2-methoxypyridine
CCOC(=O)[CH2][Zn+].[Br-]
(2-ethoxy-2-oxoethyl)zinc(II) bromide
CCOC(=O)Cc1ccnc(OC)c1
ethyl 2-(2-methoxypyridin-4-yl)acetate
Ausbeute 38.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe reaction was filtered through a course glass frit
  2. 2
    Einengenconcentrated to an oil
  3. 3
    Sonstigepurified via flash chromatography (100 g silica gel using a 5% to 50% EtOAc in heptane gradient)
  4. 4
    Einengenconcentrated

Vorschrift

Combined 4-bromo-2-methoxypyridine (654 μl, 5.32 mmol), (2-ethoxy-2-oxoethyl)zinc(II) bromide (5850 μl, 5.85 mmol), and Pd(PPh3)4 catalyst (615 mg, 0.532 mmol) in THF (15.2 mL) and heated to 120° C. in a microwave for 5 minutes. The reaction was filtered through a course glass frit, concentrated to an oil and purified via flash chromatography (100 g silica gel using a 5% to 50% EtOAc in heptane gradient). The appropriate fractions were combined and concentrated to acquire ethyl 2-(2-methoxypyridin-4-yl)acetate (400 mg, 38.5% yield) as a colorless oil. MS m/z [M+H]+ 196.1.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09345713B2uspto-grants-2016_05