반응 #65001

ord-62950ad97ad94a8d8b0720b1d8dc0bc7

반응 방정식

CC(C)(C)C1=CC(=O)C=C(C(C)(C)C)C1=O
2,6-di(tertiary-butyl)-p-benzoquinone
Nc1ccc(C(=O)O)cc1
4-aminobenzoic acid
FB(F)F
boron trifluoride
CC(C)(C)C1=CC(=Nc2ccc(C(=O)O)cc2)C=C(C(C)(C)C)C1=O
2,6-di(tertiary-butyl)-4-(4'-carboxyphenylimino)-2,5-cyclohexadien-1-one

반응 조건

온도
20°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도diethyl ether complex was heated on a steam bath for 1.25 hours
  2. 2
    기타Evaporation
  3. 3
    기타provided a solid which
  4. 4
    세척was washed with hexane
  5. 5
    기타recrystallized from ethanol

실험 절차

A mixture of 22 g (0.10 mole) of 2,6-di(tertiary-butyl)-p-benzoquinone, 13.7 g (0.10 mole) of 4-aminobenzoic acid, 175 ml of tetrahydrofuran and 1 ml of boron trifluoride: diethyl ether complex was heated on a steam bath for 1.25 hours. The mixture was allowed to cool to about 20° C. over 16 hours under a nitrogen atmosphere. Evaporation provided a solid which was washed with hexane and recrystallized from ethanol to provide orange solid 2,6-di(tertiary-butyl)-4-(4'-carboxyphenylimino)-2,5-cyclohexadien-1-one, m.p. 305°-309° C. Analysis: Calculated for C21H25NO3 : % C, 74.3; % H, 7.4; % N, 4.1; Found: % C, 74.2; % H, 7.4; % N, 4.1.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05416113uspto-grants-1995_05