Reaktion #169220

ord-76702ff425514fff805c099782e85379

Reaktionsgleichung

O=C(Cl)c1ccc(I)cc1
4-iodo-benzoyl chloride
C1CCNCC1
piperidine
O=C(c1ccc(I)cc1)N1CCCCC1
title compound
Ausbeute 100.1%
O=C(c1ccc(I)cc1)N1CCCCC1
(4-iodo-phenyl)-piperidin-1-yl-methanone
Ausbeute 100.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was heated
  2. 2
    Temperaturat reflux for 1.5 hour
  3. 3
    WaschenThe organic layer was washed with an aqueous 1M HCl solution, brine
  4. 4
    Trocknendried (Na2SO4)
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated under vacuum

Vorschrift

To a suspension of 4-iodo-benzoyl chloride (2.00 g, 7.51 mmol) in dichloromethane (25 mL) was added piperidine (1.85 mL, 18.76 mmol). The reaction mixture was heated at reflux for 1.5 hour and then cooled to room temperature. The organic layer was washed with an aqueous 1M HCl solution, brine, dried (Na2SO4), filtered, concentrated under vacuum to give the title compound (2.37 g, 100%) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846712B2uspto-grants-2014_09