반응 #1447127

ord-418285991c7942cc8a83bd07fc44e18b

반응 방정식

N#Cc1ccccc1N
anthranilonitrile
[Mg]
magnesium
CC(C)[CH2][Mg][Br]
isobutylmagnesium bromide
C1CCOC1
tetrahydrofuran
C1CCOC1
tetrahydrofuran
Cl
hydrochloric acid
CC(C)CC(=O)c1ccccc1N
1-(2-aminophenyl)-3-methylbutan-1-one
수율 25.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도At reflux
  2. 2
    온도After 5 h of heating
  3. 3
    온도under reflux
  4. 4
    기타are, at 0° C.
  5. 5
    workup.ADDITIONadded to the reaction mixture
  6. 6
    세척The organic phase is washed with water
  7. 7
    건조dried over magnesium sulphate
  8. 8
    농축Concentration
  9. 9
    기타under reduced pressure and purification on silica gel (mobile phase: petroleum ether/acetonitrile 95:5)

실험 절차

At reflux, a solution of 29.5 g (0.25 mol) of anthranilonitrile in 150 ml of tetrahydrofuran is added dropwise to a suspension comprising 18.2 g (0.75 mmol) of magnesium, 375 ml of a 2 M solution of isobutylmagnesium bromide in tetrahydrofuran and 15 ml of diethyl ether. After 5 h of heating under reflux, 100 ml of water are, at 0° C., added to the reaction mixture, and the pH is adjusted to 6 using hydrochloric acid. The organic phase is washed with water and dried over magnesium sulphate. Concentration under reduced pressure and purification on silica gel (mobile phase: petroleum ether/acetonitrile 95:5) gives 11.0 g (25% of theory) of 1-(2-aminophenyl)-3-methylbutan-1-one of logP (pH 2.3)=2.89.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07879760B2uspto-grants-2011_02