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2- 2- -2-oxocyclohexane

All the following questions concern ethyl (2 oxocyclohexane)carboxylate... [Pg.908]

Ethyl 2-oxocyclohexane-carboxylate (a cyclic 0-keto ester)... [Pg.860]

Cas/liquid reaction 8 [CL 8] Fluorination of ethyl 2-oxocyclohexane carboxylate [16] O... [Pg.609]

Synonyms AI3-00041 Anon Anone BRN 0385735 Caswell No. 270 CCRIS 5897 Cyclohexyl ketone EINECS 203-631-1 EPA pesticide chemical code 025902 Hexanon Hytrol 0 Ketocyclohexane Ketohexamethylene Nadone NCI-C55005 NSC 5711 Oxocyclohexane Pimelic ketone Pimelin ketone RCRA waste number U057 Sextone UN 1915. [Pg.332]

Oxitol, see 2-Ethoxyethanol Oxitol acetate, see 2-Ethoxyethyl acetate 2-Oxobornane, see Camphor Oxocyclohexane, see Cyclohexanone Oxolane, see Tetrahydrofuran Oxomethane, see Formaldehyde Oxybenzene, see Phenol 1,1 Oxybisbenzene, see Phenyl ether l,l -Oxybis(2-chloroethane), see Bis(2-chloroethyl) ether Oxybis(chloromethane), see s/m-Dichloromethyl ether 2,2 -Oxybis(l-chloropropane), see Bis(2-chloroisopropyl) ether... [Pg.1503]

The 4-silyl ether of a homochiral bicyclo[2.2.0]hexane-l-carboxylate was desilylated with fluoride ions in tetrahydrofuran at — 78 °C. The ensuing alkoxide cleaved the central bicyclic bond in a retro-aldol reaction to form a 4-oxocyclohexane-l-carboxylate in quantitative yield."... [Pg.547]

Ethyl 2-oxocyclohexanecarboxylate was fluorinated with l-fluoro-2,4,6-trimethylpyridiniuin triflate (1 d) and then treated with sodium hydroxide to give sodium 1 -fluoro-2-oxocyclohexane-carboxylate (21, n = 2 R = Na) in 84% yield.69... [Pg.447]

Reactions of 2-aminopyridines and diethyl 2-aryl-4-hydroxy-4-methyl-6-oxocyclohexane-l,3-dicarboxylate (309) in acetic acid for 4 h gave either ethyl 1,2-dihydro-l 1-oxo-l l//-pyrido[2,l -6]quinazoIine-2-carboxylates (310) or their isomeric ethyl 7,8-dihydro-6-oxo-6//-pyrido[l,2-a]quinazoline-8-carboxylates (311) (92PHA336). [Pg.240]

TfOH (0.6 mmol) was added dropwise to a mixture of ediyl 2-oxocyclohexane-carboxylate la (2.0 mmol) and ethyl acrylate 2a (2.4 mmol) at 0°C, and the resultant yellow mixture was allowed to stand at room temperature for 5 h. When the reaction was finished, the mixture turned brown. The cooled mixture was diluted with CH2CI2 and neutralized by the addition of the minimum amount of... [Pg.65]

See other pages where 2- 2- -2-oxocyclohexane is mentioned: [Pg.908]    [Pg.909]    [Pg.909]    [Pg.909]    [Pg.909]    [Pg.909]    [Pg.321]    [Pg.25]    [Pg.891]    [Pg.908]    [Pg.909]    [Pg.909]    [Pg.909]    [Pg.909]    [Pg.909]    [Pg.230]    [Pg.898]    [Pg.915]    [Pg.916]    [Pg.916]    [Pg.916]    [Pg.916]    [Pg.916]    [Pg.2280]    [Pg.2280]    [Pg.2500]    [Pg.2500]    [Pg.2500]    [Pg.2500]    [Pg.2500]    [Pg.2500]    [Pg.2538]    [Pg.334]    [Pg.576]    [Pg.585]    [Pg.586]    [Pg.586]    [Pg.586]   
See also in sourсe #XX -- [ Pg.1544 ]



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2- Oxocyclohexane-carboxylic acid

2-Oxocyclohexane carboxylic derivatives

Ethyl 2-oxocyclohexane carboxylate

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