반응 #543546

ord-1d55ecfb0ec9447baf09db486c82d860

반응 방정식

CC(=O)O
acetic acid
Nc1ccc(-c2ccc(N)c(N)c2)cc1N
3,3′-diaminobenzidine
CC(C)=N.Nc1ccc(-c2ccc(N)c(N)c2)cc1N
3,3′-diaminobenzidine monoisopropanimine
CC(C)=N.CC(C)=N.Nc1ccc(-c2ccc(N)c(N)c2)cc1N
3,3′-diaminobenzidine diisopropanimine

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타In a 200-ml flask equipped with a Soxhlet extractor
  2. 2
    온도by heating
  3. 3
    온도under reflux in a nitrogen atmosphere for 3 hours
  4. 4
    기타acetone was removed under reduced pressure
  5. 5
    기타the residue was purified by silica gel chromatography

실험 절차

In a 200-ml flask equipped with a Soxhlet extractor including molecular sieves 4A as a dehydrating agent, a stirrer, a condenser and a thermometer were placed 21.4 g (100 mmol) of 3,3′-diaminobenzidine, 100 ml of acetone and 3.0 g (50 mmol) of acetic acid, followed by heating under reflux in a nitrogen atmosphere for 3 hours. After cooling to room temperature, acetone was removed under reduced pressure, and the residue was purified by silica gel chromatography to yield 16.5 g (65 mmol) of 3,3′-diaminobenzidine monoisopropanimine [N′-isopropylidene-3,4,3′,4′-biphenyltetramine] and 4.7 g (16 mmol) of 3,3′-diaminobenzidine diisopropanimine [N′,N′″-diisopropylidene-3,4,3′,4′-biphenyltetramine].

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07186454B2uspto-grants-2007_03