반응 #1876816

ord-587fa6dd1dba43fda10d118c83fddfdf

반응 방정식

CC(=O)Cl
acetylchloride
Nc1ccccc1C(=O)c1ccccc1
2-Aminobenzophenone
CCN(CC)CC
triethylamine
Clc1cc(-c2ccccc2)c2ccccc2n1
2-Chloro-4-phenylquinoline
CC(=O)Nc1ccccc1C(=O)c1ccccc1
2-acetamidobenzophenone

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The reaction mixture was then removed from ice
  2. 2
    workup.ADDITIONUpon the addition of 10% hydrochloric acid (84 mL)
  3. 3
    추출extracted with ethyl acetate
  4. 4
    건조dried with magnesium sulfate
  5. 5
    농축concentrated
  6. 6
    기타Purification by column chromatography (25% ethyl acetate/heptane)

실험 절차

2-Chloro-4-phenylquinoline was prepared by the following method (Rxn-1). 2-Aminobenzophenone (21 g, 106.5 mmol) was dissolved in methylene chloride (213 mL) and triethylamine (22.3 mL, 159.8 mmol) was added slowly. After cooling to 0° C., acetylchloride (8.3 mL, 117.2 mmol) was added to the reaction mixture dropwise. The reaction mixture was then removed from ice and allowed to stir overnight. Upon the addition of 10% hydrochloric acid (84 mL), the aqueous layers were combined and extracted with ethyl acetate. The organic phases were combined, dried with magnesium sulfate, and concentrated. Purification by column chromatography (25% ethyl acetate/heptane) gave 2-acetamidobenzophenone.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07070868B2uspto-grants-2006_07