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Conditions | Yield |
---|---|
With 6C6H15P*4CF3O3S(1-)*2Ru(2+); acetone In 2,2,2-trifluoroethanol at 20℃; for 3h; Reagent/catalyst; | 99% |
With tetra-O-acetyl riboflavin; lithium trifluoromethanesulfonate; 1,3-diisopropylthiourea In water; acetonitrile at 22℃; for 24h; Inert atmosphere; Sealed tube; Irradiation; | 90% |
With isobutyl 4-[bis(acetoxy)iodo]phenylsulfonate; ruthenium trichloride In water; acetonitrile at 20℃; for 8h; | 89% |
cyclohexanylcarbonyl chloride
cyclohexyltrifluoro-λ4-borane potassium salt
dicyclohexyl ketone
Conditions | Yield |
---|---|
With potassium fluoride; (1,2-dimethoxyethane)dichloronickel(II); Ir(dF(CF3)ppy)2(bpy)PF6; 4,4'-di-tert-butyl-2,2'-bipyridine In 1,2-dimethoxyethane at 24℃; for 24h; Inert atmosphere; Sealed tube; Irradiation; | 84% |
tricyclohexylborane
lithium tris(phenylthio)methanide
dicyclohexyl ketone
Conditions | Yield |
---|---|
With sodium hydroxide; dihydrogen peroxide Ambient temperature; | 80% |
Conditions | Yield |
---|---|
With tetraethyl ammonium permanganate at 20℃; for 0.666667h; | 80% |
Conditions | Yield |
---|---|
With air; sodium nitrite In trifluoroacetic acid at 0 - 20℃; for 5h; | A 79% B n/a |
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; chloro-trimethyl-silane; nickel(II) bromide 2-methoxyethyl ether complex; zinc In tetrahydrofuran; N,N-dimethyl acetamide at 40℃; for 2h; Sealed tube; Inert atmosphere; | 76% |
2'-cyclohexyl-2'-phenylsulfinylspiro
dicyclohexyl ketone
Conditions | Yield |
---|---|
With sodium phenylselenide In ethanol for 16h; Heating; | 75% |
With sodium phenylselenide In ethanol for 16h; Heating; | 75% |
Conditions | Yield |
---|---|
In tetrahydrofuran at -80 - 20℃; Inert atmosphere; | 75% |
1,1-Diphenylmethanol
A
dicyclohexyl ketone
B
Dicyclohexylmethanol
C
cyclohexylphenylmethanol
Conditions | Yield |
---|---|
With hydrogen In water at 50℃; under 15001.5 Torr; for 6h; chemoselective reaction; | A 7 %Spectr. B 75% C 17% |
dicyclohexylacetic acid
dicyclohexyl ketone
Conditions | Yield |
---|---|
With (2,2'-dipyridyl)bis(5-methyl-2-(4-fluoro)phenylpyridine-N,C)iridium(III) hexafluorophosphate; oxygen; sodium carbonate; 1,1'-diethyl-4,4'-bipyridinium diperchlorate In dimethyl sulfoxide at 20℃; under 760.051 Torr; for 16h; Irradiation; | 65% |
Conditions | Yield |
---|---|
Stage #1: 1-bromocyclohexane With magnesium In tetrahydrofuran at 20℃; for 1h; Stage #2: cyclohexanecarbaldehyde In tetrahydrofuran at 0 - 20℃; for 2h; Stage #3: With 1,3-Diiodo-5,5-dimethyl-2,4-imidazolidinedione; potassium carbonate In tetrahydrofuran; tert-butyl alcohol for 20h; Reflux; Darkness; | 60% |
Conditions | Yield |
---|---|
With (1,2-dimethoxyethane)dichloronickel(II); [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; potassium carbonate; 4,4'-di-tert-butyl-2,2'-bipyridine In benzene at 20℃; for 16h; Irradiation; Inert atmosphere; | 60% |
With potassium phosphate; sodium tungstate (VI) dihydrate; [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; Ni[(4,4′-di-tert-butyl-2,2′-bipyridine)(H2O)4]Cl2; lithium chloride In benzene at 20℃; for 24h; Inert atmosphere; Sealed tube; Schlenk technique; Irradiation; | 52% |
cyclohexanecarboxylic acid anhydride
dicyclohexyl ketone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; (1,2-dimethoxyethane)dichloronickel(II); Ir[dF(OMe)ppy]2-(dtbbpy)PF6; 1,8-diazabicyclo[5.4.0]undec-7-ene In 1,4-dioxane at 25℃; for 36h; Sealed tube; Inert atmosphere; Irradiation; | 50% |
Conditions | Yield |
---|---|
With potassium iodide In N,N-dimethyl-formamide at 80℃; for 20h; | 47% |
trimethyl<<(1Z)-1-cyclohexylhepta-1,6-dienyl>oxy>silane
dicyclohexyl ketone
Conditions | Yield |
---|---|
With 9,10-Dicyanoanthracene In acetonitrile for 120h; Irradiation; | 37% |
With 9,10-Dicyanoanthracene In acetonitrile for 65h; Irradiation; | 37 % Chromat. |
2,6-diisopropylphenyl isocyanate
A
dicyclohexyl ketone
Conditions | Yield |
---|---|
With Ru photocatalyst; Ni catalyst In N,N-dimethyl-formamide Mechanism; Irradiation; | A n/a B 16% |
Conditions | Yield |
---|---|
Stage #1: cyclohexylmagnesiumchloride With titanium(IV) isopropylate In diethyl ether at -78 - -30℃; for 0.166667h; Stage #2: carbon dioxide In diethyl ether at -30 - 0℃; for 0.25h; Stage #3: With iodine In diethyl ether at 20℃; for 2h; | A 14% B 0.12 g |
cyclohexane
carbon monoxide
A
dicyclohexyl ketone
B
Cyclohexyl methyl ketone
C
cyclohexanecarbaldehyde
D
Cyclohexanecarboxylic acid
Conditions | Yield |
---|---|
With tris(tetrabutylammonium)12-tungstophosphate In acetonitrile at 25℃; under 760 Torr; for 16h; Product distribution; Mechanism; Irradiation; other alkanes and aromatic reactants; var. solvents and times; | A 4.1 % Turnov. B 2.7 % Turnov. C 8% D n/a |
diethyl ether
ethyl cyclohexanecarboxylate
cyclohexylmagnesiumchloride
A
cyclohexylcyclohexane
B
dicyclohexyl ketone
C
α,α-dicyclohexyl-cyclohexanemethanol
cyclohexyl chloride
ethyl cyclohexanecarboxylate
A
dicyclohexyl ketone
B
α,α-dicyclohexyl-cyclohexanemethanol
Conditions | Yield |
---|---|
With diethyl ether; magnesium | |
With sodium; pentane |
Conditions | Yield |
---|---|
With diethyl ether; cyclohexylmagnesiumchloride | |
With diethyl ether; tert.-butyl lithium | |
With tert.-butyl lithium In diethyl ether Heating; |
exifone
dicyclohexyl ketone
Conditions | Yield |
---|---|
With ethyl acetate; platinum Hydrogenation; |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With oxalyl dichloride | |
With cyclohexanylcarbonyl chloride | |
Multi-step reaction with 3 steps 1: benzene 2: KOH-solution 3: concentrated sulfuric acid View Scheme |
1,1-Dicyclohexyl-2-methoxy-ethanol
dicyclohexyl ketone
Conditions | Yield |
---|---|
(electrochemical oxidation); |
Dicyclohexyl-chlor-methylboronsaeuredimethylester
dicyclohexyl ketone
Conditions | Yield |
---|---|
With sodium hydroxide; dihydrogen peroxide |
1-Cyclohexanecarbonyl-cyclohexanecarboxylic acid; compound with diisopropyl-amine
dicyclohexyl ketone
Conditions | Yield |
---|---|
at 150 - 200℃; |
Conditions | Yield |
---|---|
(i) THF, (ii) aq. NaOH, H2O2; Multistep reaction; |
α-picoline
dicyclohexyl ketone
1,1-dicyclohexyl-2-(pyridin-2-yl)ethanol
Conditions | Yield |
---|---|
Stage #1: α-picoline With n-butyllithium In tetrahydrofuran; hexane at -78 - -20℃; Inert atmosphere; Stage #2: dicyclohexyl ketone In tetrahydrofuran; hexane at -20℃; Inert atmosphere; Stage #3: With water; ammonium chloride In tetrahydrofuran; hexane | 100% |
4-Phenyl-1-butyne
dicyclohexyl ketone
1,1-dicyclohexyl-5-phenyl-2-pentyn-1-ol
Conditions | Yield |
---|---|
Stage #1: 4-Phenyl-1-butyne With n-butyllithium In tetrahydrofuran; hexanes at -78℃; for 1h; Stage #2: dicyclohexyl ketone In tetrahydrofuran; hexanes at -78 - 20℃; for 3.5h; | 100% |
Conditions | Yield |
---|---|
With (N,N'-dicyclohexyl-2H-imidazol-2-ylidene)CuCl; sodium t-butanolate In toluene at 80℃; for 0.5h; | 99% |
With sodium t-butanolate; [CuCl(N,N'-bis(cyclohexyl)imidazol-2-ylidene)] In toluene at 80℃; for 0.5h; | 99% |
With (1,3-bis(9-ethyl-9H-fluoren-9-yl)imidazol-2-ylidene)copper(I) chloride; potassium tert-butylate In tetrahydrofuran at 65℃; for 4h; Catalytic behavior; Solvent; Time; Reagent/catalyst; Temperature; Inert atmosphere; Schlenk technique; | 98% |
dicyclohexyl ketone
Conditions | Yield |
---|---|
With sodium borodeuteride In methanol at 25℃; for 2h; Cooling with ice; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
Stage #1: dicyclohexyl ketone With bis-{[N,N′-bis(2,6-(di-isopropyl)phenyl)imidazol-2-ylidene]-(1H-1,2,4-triazol-1-yl)}copper(I) In tetrahydrofuran at 55℃; for 14h; Stage #2: With sodium hydroxide In methanol; water at 25℃; for 1.5h; | 97% |
With methanol; sodium tetrahydroborate at 0 - 20℃; | 96% |
With methanol; sodium tetrahydroborate at 0 - 20℃; | 96% |
Conditions | Yield |
---|---|
In tetrahydrofuran; hexane at -78℃; for 5h; | 96% |
dicyclohexyl ketone
trimethylsilylacetylene
1,1-dicyclohexylprop-2-yn-1-ol
Conditions | Yield |
---|---|
Stage #1: trimethylsilylacetylene With n-butyllithium In tetrahydrofuran; hexane at -10℃; for 1h; Inert atmosphere; Stage #2: dicyclohexyl ketone In tetrahydrofuran; hexane at -10 - 0℃; for 3h; Inert atmosphere; Stage #3: With sodium hydroxide In tetrahydrofuran; methanol; hexane at 0 - 20℃; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
With Montmorillonite clay KSF at 110℃; for 0.25h; Irradiation; | 92% |
chloro-trimethyl-silane
dicyclohexyl ketone
Dicyclohexyltrimethylsilylenolether
Conditions | Yield |
---|---|
With lithium hexamethyldisilazane | 92% |
Conditions | Yield |
---|---|
With Montmorillonite clay KSF at 75℃; for 0.0333333h; Irradiation; | 91% |
triethylsilane
dicyclohexyl ketone
A
(cyclohexylidenemethyl)cyclohexane
Conditions | Yield |
---|---|
With [(SIMes)PFMe2][B(C6F5)4]2 In dichloromethane-d2 at 20℃; for 1h; Temperature; Reagent/catalyst; Inert atmosphere; Schlenk technique; Glovebox; | A 11% B 89% |
dicyclohexyl ketone
1,2-dichlorovinyl phenyl ether
Conditions | Yield |
---|---|
Stage #1: 1,2-dichlorovinyl phenyl ether With n-butyllithium In diethyl ether; hexane at -78 - -20℃; for 2h; Stage #2: dicyclohexyl ketone In diethyl ether; hexane at -78 - 20℃; | 88% |
dicyclohexyl ketone
1,2-Epoxy-3-bromopropane
4-Bromomethyl-2,2-dicyclohexyl-[1,3]dioxolane
Conditions | Yield |
---|---|
With tin(IV) chloride In tetrachloromethane for 2.5h; Ambient temperature; | 86.8% |
Conditions | Yield |
---|---|
With Fe3O4(at)cellulose-OSO3H nanocomposite In ethanol at 20℃; for 1.5h; Green chemistry; | 85% |
Conditions | Yield |
---|---|
Stage #1: 1-Pentyne With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Inert atmosphere; Stage #2: dicyclohexyl ketone In tetrahydrofuran; hexane at -78 - 20℃; for 3h; Inert atmosphere; | 85% |
dicyclohexyl ketone
1-phenyl-2-bromoethane
1,1-dicyclohexyl-3-phenyl-propan-1-ol
Conditions | Yield |
---|---|
Stage #1: 1-phenyl-2-bromoethane With magnesium In tetrahydrofuran at -20℃; for 1h; Inert atmosphere; Stage #2: dicyclohexyl ketone In tetrahydrofuran at 20℃; for 3.25h; | 84% |
Conditions | Yield |
---|---|
Stage #1: 3,4-dihydro-2H-pyran With n-butyllithium In tetrahydrofuran; hexane at 0 - 20℃; for 3.16667h; Inert atmosphere; Stage #2: dicyclohexyl ketone In tetrahydrofuran; hexane at -78 - 20℃; for 2h; | 83% |
Conditions | Yield |
---|---|
Stage #1: 2-(tert-butyldimethylsilyloxy)ethyl bromide With magnesium In diethyl ether at 25℃; for 1h; Inert atmosphere; Stage #2: dicyclohexyl ketone In diethyl ether for 3h; Inert atmosphere; | 82.2% |
1,3-Benzothiazole
dicyclohexyl ketone
1-(2-benzothiazolyl)-1,1-dicyclohexylmethanol
Conditions | Yield |
---|---|
Stage #1: 1,3-Benzothiazole; dicyclohexyl ketone With tetrakis{[tris(dimethylamino)phosphoranyliden]amino}phosphonium fluoride; tris(trimethylsilyl)amine In toluene at 20℃; for 24h; Inert atmosphere; Stage #2: In tetrahydrofuran | 82% |
dicyclohexyl ketone
3-(benzotriazol-1-yl)-3-ethoxy-1-propene
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran 1.) -78 deg C, 10 min, 2.) -78 deg C, 3 h; 20 deg C, 12 h; | 81% |
dicyclohexyl ketone
A
(cyclohexylidenemethyl)cyclohexane
B
dicyclohexylmethane
Conditions | Yield |
---|---|
With triethylsilane; [(SIMes)PFMe2][B(C6F5)4]2 In dichloromethane-d2 at 50℃; for 24h; Temperature; Reagent/catalyst; Inert atmosphere; Glovebox; Schlenk technique; | A 19% B 81% |
dicyclohexyl ketone
A
1,5-dicyclohexyl-1H-tetrazole
B
1-cyclohexyl-5-cyclohexylaminotetrazole
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; trimethylsilylazide In dichloromethane at 20℃; for 5h; Inert atmosphere; regioselective reaction; | A 80% B 12% |
dicyclohexyl ketone
Conditions | Yield |
---|---|
With naphthalene; lithium In tetrahydrofuran for 6.5h; McMurry olefination; Heating; | 78% |
With titanium(III) chloride In tetrahydrofuran 1.) reflux, 1 h, 2.) reflux, 10 h; | 20% |
dicyclohexyl ketone
Methyltriphenylphosphonium bromide
ethene-1,1-diyldicyclohexane
Conditions | Yield |
---|---|
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran at 0℃; for 2.75h; Inert atmosphere; Stage #2: dicyclohexyl ketone In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 78% |
Stage #1: Methyltriphenylphosphonium bromide With sodium hexamethyldisilazane; sodium t-butanolate In tetrahydrofuran at 0℃; for 0.5h; Stage #2: dicyclohexyl ketone In tetrahydrofuran at 20℃; | 75% |
Stage #1: Methyltriphenylphosphonium bromide With sodium hexamethyldisilazane In tetrahydrofuran at 0℃; for 1h; Stage #2: dicyclohexyl ketone In tetrahydrofuran at 0 - 20℃; | 41% |
With n-butyllithium In tetrahydrofuran at 0 - 20℃; for 48h; | |
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran at 0 - 20℃; for 3h; Inert atmosphere; Stage #2: dicyclohexyl ketone at 0 - 20℃; for 48h; Inert atmosphere; |
Conditions | Yield |
---|---|
With lithium tert-butoxide In chloroform at 25℃; for 0.5h; Atherton-Todd Synthesis; | 76% |
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