FI (list display)

  • C07C37/00
  • Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring HB CC 4H006
  • C07C37/01
  • .by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis [3] HB CC 4H006
  • C07C37/02
  • ..by substitution of halogen [3] HB CC 4H006
  • C07C37/04
  • ..by substitution of SO3H groups or a derivative thereof [3] HB CC 4H006
  • C07C37/045
  • ..by substitution of a group bound to the ring by nitrogen [3] HB CC 4H006
  • C07C37/05
  • ...by substitution of a NH2 group [3] HB CC 4H006
  • C07C37/055
  • ..by substitution of a group bound to the ring by oxygen, e.g. ether group [3] HB CC 4H006
  • C07C37/06
  • .by conversion of non-aromatic six-membered rings or of such rings formed in situ into aromatic six-membered rings, e.g. by dehydrogenation HB CC 4H006
  • C07C37/07
  • ..with simultaneous reduction of C=O group in that ring [3] HB CC 4H006
  • C07C37/08
  • .by decomposition of hydroperoxides, e.g. cumene hydroperoxide HB CC 4H006
  • C07C37/11
  • .by reactions increasing the number of carbon atoms [3] HB CC 4H006
  • C07C37/14
  • ..by addition reactions, i.e. reactions involving at least one carbon-to-carbon unsaturated bond [3] HB CC 4H006
  • C07C37/16
  • ..by condensation involving hydroxy groups of phenols or alcohols or the ether or mineral ester group derived therefrom [3] HB CC 4H006
  • C07C37/18
  • ..by condensation involving halogen atoms of halogenated compounds HB CC 4H006
  • C07C37/20
  • ..using aldehydes or ketones HB CC 4H006
  • C07C37/48
  • .by exchange of hydrocarbon groups which may be substituted, from other compounds, e.g. transalkylation [3] HB CC 4H006
  • C07C37/50
  • .by reactions decreasing the number of carbon atoms (C07C 37/01, C07C 37/08, C07C 37/48 take precedence) [3] HB CC 4H006
  • C07C37/52
  • ..by splitting polyaromatic compounds, e.g. polyphenolalkanes [3] HB CC 4H006
  • C07C37/54
  • ...by hydrolysis of lignin or sulfite waste liquor [3] HB CC 4H006
  • C07C37/56
  • ..by replacing a carboxyl or aldehyde group by a hydroxy group [3] HB CC 4H006
  • C07C37/58
  • .by oxidation reactions introducing directly a hydroxy group on a CH-group belonging to a six-membered aromatic ring with the aid of molecular oxygen [3] HB CC 4H006
  • C07C37/60
  • .by oxidation reactions introducing directly a hydroxy group on a CH-group belonging to a six-membered aromatic ring with the aid of other oxidants than molecular oxygen or their mixtures with molecular oxygen [3] HB CC 4H006
  • C07C37/62
  • .by introduction of halogen; by substitution of halogen atoms by other halogen atoms [3] HB CC 4H006
  • C07C37/64
  • .Preparation of O-metal compounds with the O-metal group linked to a carbon atom belonging to a six-membered aromatic ring [3] HB CC 4H006
  • C07C37/66
  • ..by conversion of hydroxy groups to O-metal groups [3] HB CC 4H006
  • C07C37/68
  • .Separation; Purification; Stabilisation; Use of additives [3] HB CC 4H006
  • C07C37/70
  • ..by physical treatment [3] HB CC 4H006
  • C07C37/72
  • ...by liquid-liquid treatment [3] HB CC 4H006
  • C07C37/74
  • ...by distillation [3] HB CC 4H006
  • C07C37/76
  • ....by steam distillation [3] HB CC 4H006
  • C07C37/78
  • ....by azeotropic distillation [3] HB CC 4H006
  • C07C37/80
  • ....by extractive distillation [3] HB CC 4H006
  • C07C37/82
  • ...by solid-liquid treatment; by chemisorption [3] HB CC 4H006
  • C07C37/84
  • ...by crystallisation [3] HB CC 4H006
  • C07C37/86
  • ..by treatment giving rise to a chemical modification (by chemisorption C07C 37/82) [3] HB CC 4H006
  • C07C37/88
  • ..Use of additives, e.g. for stabilisation [3] HB CC 4H006
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