Reaktion #61747

ord-ee91f2fb4d5d444dba1ba278f1df6b08

Reaktionsgleichung

O=[N+]([O-])c1cc(CO)ccc1F
(4-fluoro-3-nitro-phenyl)-methanol
CC1CCNCC1
4-methyl piperidine
C1COCCN1
morpholine
CC1CCN(c2ccc(CO)cc2[N+](=O)[O-])CC1
[4-(4-methyl-piperidin-1-yl)-3-nitro-phenyl]-methanol

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction was evaporated onto celite
  2. 2
    Sonstigepurified by flash chromatography

Vorschrift

A stirred suspension of (4-fluoro-3-nitro-phenyl)-methanol (171 mg, 1 mmol), 4-methyl piperidine (95 mg, 0.96 mmol) PS morpholine (400 mg, 1 mmol), and chloroform (3 mL) was heated at 50° C. for 2 hrs. The reaction was evaporated onto celite and purified by flash chromatography to give [4-(4-methyl-piperidin-1-yl)-3-nitro-phenyl]-methanol (i). 1H NMR (CDCl3, 300 MHz): δ 7.8 (s, 1H), 7.4 (d, 1H), 7.1 (d, 1H), 4.6 (s, 2H), 3.2 (d, 2H), 2.8 (dd, 2H), 1.8-1.3 (m, 5H), 1.0 (d, 3H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07429603B2uspto-grants-2008_09