반응 #581039

ord-9ecf00a1c6d940d2895486a26ff8f69e

반응 방정식

Cl
HCl
N#Cc1ccc(Cl)cc1N
2-amino-4-chlorobenzonitrile
CCOCC
Et2O
[CH3][Mg][Cl]
MeMgCl
Cl
HCl
CC(=O)c1ccc(Cl)cc1N
title material
CC(=O)c1ccc(Cl)cc1N
1-(2-amino-4-chlorophenyl)ethanone

반응 조건

온도
-60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGStirring
  2. 2
    기타was removed
  3. 3
    workup.STIRRINGthe reaction stirred for 21 h at rt
  4. 4
    온도to warm slowly to rt within the cooling bath
  5. 5
    기타The Et2O layer was separated
  6. 6
    workup.ADDITIONby addition of solid KOH
  7. 7
    추출later extracted with EtOAc (3×)
  8. 8
    건조dried (Na2SO4)
  9. 9
    농축concentrated under reduced pressure

실험 절차

To a vigourosly stirred, Et2O (100 mL) solution of 2-amino-4-chlorobenzonitrile (1.00 g, 6.55 mmol) cooled in an ice-H2O bath was added MeMgCl (3.0 M in THF, 6.5 mL, 19.7 mmol) dropwise over 5 min. During that time the reaction became a thick yellow suspension. Stirring was continued at the temperature for 1 h before the cooling bath was removed and the reaction stirred for 21 h at rt. The resultant light yellow suspension cooled to −60° C. and treated with aq HCl (5 M, 8 mL, 40 mmol) dropwise over 3 min. The mixture was allowed to warm slowly to rt within the cooling bath. Later more aq HCl (5 M, 6.5 mL, 33 mmol) was added. The Et2O layer was separated, the aq phase was basicified (pH 4-5) by addition of solid KOH and later extracted with EtOAc (3×). The Et2O and EtOAc layers were combined, dried (Na2SO4) and concentrated under reduced pressure to afford the title material which was used without further purification; 1H NMR (400 MHz, CDCl3) δ 7.63 (d, J=8.4 Hz, 1H), 6.65 (d, J=2.0 Hz, 1H), 6.60 (dd, J=2.0 Hz, 8.0 Hz, 1H), 6.40 (br, 2H), 2.55 (s, 3H); MS (ES+): m/z 170.07 (100) [MH+]; HPLC: tR=3.12 min (OpenLynx, polar—5 min).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07534797B2uspto-grants-2009_05