(0)C07C:17/49:
IPC6
SECTION C - CHEMISTRY; METALLURGY
ACYCLIC OR CARBOCYCLIC COMPOUNDS
C07C
18/50
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/ 00 Quinones (for quinone methides, see unsaturated ketones with a keto group being part of a ring) [3]

Note

 

In this group, quinhydrones are classified according to their quinoid part. [3]

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/ 02 • with monocyclic quinoid structure [3]  

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/ 04 • • Benzoquinones, i.e. C6H4O2 [3]  

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/ 06 • • with unsaturation outside the quinoid structure [3]  

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/ 08 • with polycyclic non-condensed quinoid structure [3]  

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/ 10 • the quinoid structure being part of a condensed ring system containing two rings [3]  

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/ 12 • • Naphthoquinones, i.e. C10H6O2 [3]  

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/ 14 • • with unsaturation outside the ring system, e.g. vitamin K1 [3]  

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/ 16 • the quinoid structure being part of a condensed ring system containing three rings [3]  

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/ 18 • • Anthraquinones, i.e. C14H8O2 [3]  

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/ 20 • • with unsaturation outside the ring system [3]  

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/ 22 • the quinoid structure being part of a condensed ring system containing four or more rings [3]  

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/ 24 • containing halogen [3]  

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/ 26 • containing groups having oxygen atoms singly bound to carbon atoms [3]  

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/ 28 • • with monocyclic quinoid structure [3]  

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/ 30 • • with polycyclic non-condensed quinoid structure [3]  

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/ 32 • • the quinoid structure being part of a condensed ring system having two rings [3]  

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/ 34 • • the quinoid structure being part of a condensed ring system having three rings [3]  

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/ 36 • • the quinoid structure being part of a condensed ring system having four or more rings [3]  

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/ 38 • containing —CHO or non-quinoid keto groups [3]  
 

51
/ 00 Preparation of carboxylic acids or their salts, halides, or anhydrides (of acids by hydrolysis of oils, fats, or waxes C 11 C) [2]

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/ 02 • from salts of carboxylic acids  

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/ 04 • from carboxylic acid halides  

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/ 06 • from carboxylic acid amides  

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/ 08 • from nitriles  

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/ 083 • from carboxylic acid anhydrides [3]  

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/ 087 • • by hydrolysis [3]  

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/ 09 • from carboxylic acid esters or lactones (saponification of carboxylic acid esters C 07 C 27/02)  

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/ 093 • by hydrolysis of —CX3 groups, X being halogen [3]  

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/ 097 • from or via nitro-substituted organic compounds [3]  

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/ 10 • by reaction with carbon monoxide  

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/ 12 • • on an oxygen-containing group in organic compounds, e.g. alcohols  

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/ 14 • • on a carbon-to-carbon unsaturated bond in organic compounds [3]  

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/ 145 • • with simultaneous oxidation [3]  

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/ 15 • by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis [2]  

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/ 16 • by oxidation (C 07 C 51/145 takes precedence) [3]  

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/ 21 • • with molecular oxygen [3]  

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/ 215 • • • of saturated hydrocarbyl groups [3]  

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/ 225 • • • • of paraffin waxes [3]  

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/ 23 • • • of oxygen-containing groups to carboxyl groups [3]  

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/ 235 • • • • of —CHO groups or primary alcohol groups [3]  

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/ 245 • • • • of keto groups or secondary alcohol groups [3]  

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/ 25 • • • of unsaturated compounds containing no six-membered aromatic ring [3]  

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/ 255 • • • of compounds containing six-membered aromatic rings without ring-splitting [3]  

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/ 265 • • • • having alkyl side chains which are oxidised to carboxyl groups [3]  

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/ 27 • • with oxides of nitrogen or nitrogen-containing mineral acids [3]  

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/ 275 • • • of hydrocarbyl groups [3]  

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/ 285 • • with peroxy-compounds [3]  

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/ 29 • • with halogen-containing compounds which may be formed in situ [3]  

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/ 295 • • with inorganic bases, e.g. by alkali fusion [3]  

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/ 305 • • with sulfur or sulfur-containing compounds [3]  

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/ 31 • • of cyclic compounds with ring-splitting [3]  

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/ 34 • by oxidation with ozone; by hydrolysis of ozonides [3]  

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/ 347 • by reactions not involving formation of carboxyl groups [3]  

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/ 353 • • by isomerisation; by change of size of the carbon skeleton [3]  

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/ 36 • • by hydrogenation of carbon-to-carbon unsaturated bonds [3]  

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/ 363 • • by introduction of halogen; by substitution of halogen atoms by other halogen atoms [3]  

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/ 367 • • by introduction of functional groups containing oxygen only in singly bound form [3]  

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/ 373 • • by introduction of functional groups containing oxygen only in doubly bound form [3]  

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/ 377 • • by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups [3]  

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/ 38 • • • by decarboxylation [3]  

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/ 41 • Preparation of salts of carboxylic acids by conversion of the acids or their salts into salts with the same carboxylic acid part (preparation of soap C 11 D) [3]  

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/ 42 • Separation; Purification; Stabilisation; Use of additives [3]  

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/ 43 • • by change of the physical state, e.g. crystallisation [3]  

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/ 44 • • • by distillation [3]  

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/ 46 • • • • by azeotropic distillation [3]  

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/ 47 • • by solid-liquid treatment; by chemisorption [3]  

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/ 48 • • by liquid-liquid treatment  

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/ 487 • • by treatment giving rise to chemical modification (by chemisorption C 07 C 51/47) [3]  

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/ 493 • • • whereby carboxylic acid esters are formed [3]  

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/ 50 • • Use of additives, e.g. for stabilisation [3]  

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/ 54 • Preparation of carboxylic acid anhydrides (by oxidation C 07 C 51/16)  

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/ 56 • • from organic acids, their salts, or their esters  

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/ 567 • • by reactions not involving the carboxylic acid anhydride group [3]  

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/ 573 • • Separation; Purification; Stabilisation; Use of additives [3]  

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/ 58 • Preparation of carboxylic acid halides  

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/ 60 • • by conversion of carboxylic acids or their anhydrides into halides with the same carboxylic acid part [3]  

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/ 62 • • by reactions not involving the carboxylic acid halide group [3]  

51
/ 64 • • Separation; Purification; Stabilisation; Use of additives [3]  

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