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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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inquiryBICYCLO[3.2.1]OCTAN-2-ONE Basic information Product Name: BICYCLO[3.2.1]OCTAN-2-ONE
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Supply top quality products with a reasonable price Application:api
Conditions | Yield |
---|---|
With chromium(VI) oxide; acetic acid | 79% |
Conditions | Yield |
---|---|
With chromium(VI) oxide; acetic acid | |
With pyridine; chromium(VI) oxide |
bicyclo[3.2.1]oct-2-ene
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
(i) (UV-irradiation), toluene, AcOH, (ii) LiAlH4, Et2O, (iii) CrO3, aq. H2SO4; Multistep reaction; |
optically inactive 6-hydroxy-bicyclo[3.2.1]octane
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
With chromium(VI) oxide |
N-Aethoxycarbonyl-2-(4-oxo-cyclohexyl)-aethylamin
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
(i) N2O4, (ii) K2CO3, MeOH, CH2Cl2; Multistep reaction; |
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
(oxidation); |
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
(i) Hg(OAc)2, aq. AcOH, (ii) H2S; Multistep reaction; |
(1S,2S,4S,5R)-Tricyclo[3.2.1.02,4]octan-2-ol
A
bicyclo[3.2.1]octan-2-one
B
3-methylbicyclo[2.2.1]heptan-2-one
Conditions | Yield |
---|---|
With potassium tert-butylate In tert-butyl alcohol at 25℃; for 0.166667h; | A 90 % Chromat. B 10 % Chromat. |
With potassium tert-butylate In tert-butyl alcohol at 82℃; for 0.166667h; | A 85 % Chromat. B 15 % Chromat. |
A
bicyclo[3.2.1]octan-3-one
B
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
With sodium hydroxide; hydroxy(tosyloxy)iodobenzene; iodine 1.) CH3CN, rt., 18 h; 2.) CH3OH, 24 h, reflux; Yield given. Multistep reaction. Yields of byproduct given; |
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
With potassium dichromate; sulfuric acid |
A
bicyclo[3.2.1]octan-2-one
endo-bicyclo<3.2.1>-octan-2-ol
Conditions | Yield |
---|---|
With methanol; Pd-BaSO4 Hydrogenation; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 92 percent / tetrahydrofuran / Ambient temperature 2: N-iodosuccinimide, AgNO3 / acetone / Ambient temperature 3: 1.) iodine, benzene; 2.) aq. NaOH / 1.) CH3CN, rt., 18 h; 2.) CH3OH, 24 h, reflux View Scheme |
2-exo-ethynylbicyclo<2.2.1>heptan-2-ol
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: N-iodosuccinimide, AgNO3 / acetone / Ambient temperature 2: 1.) iodine, benzene; 2.) aq. NaOH / 1.) CH3CN, rt., 18 h; 2.) CH3OH, 24 h, reflux View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 75 percent / aq. NaOH, H2 / 10percent Pd/C / tetrahydrofuran / 1.5 h 2: 79 percent / CrO3, AcOH View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: benzene 2: Na / butan-2-ol 3: (oxidation) View Scheme |
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2 / Pd-C / ethanol 2: (i) N2O4, (ii) K2CO3, MeOH, CH2Cl2 View Scheme |
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Na / butan-2-ol 2: (oxidation) View Scheme |
Conditions | Yield |
---|---|
With ethylenediamine for 8h; Heating; | 94% |
bicyclo[3.2.1]octan-2-one
bicyclo<3.2.1>octan-2-one oxime
Conditions | Yield |
---|---|
With potassium hydroxide; hydroxylamine hydrochloride In ethanol; water for 4h; Heating; | 93% |
N,N-phenylbistrifluoromethane-sulfonimide
bicyclo[3.2.1]octan-2-one
2-trifluoromethanesulfonyloxybicyclo[3.2.1]oct-2-ene
Conditions | Yield |
---|---|
With n-butyllithium; diisopropylamine In tetrahydrofuran | 87% |
Conditions | Yield |
---|---|
With triethylamine; sodium iodide In acetonitrile; pentane Ambient temperature; | 81% |
bicyclo[3.2.1]octan-2-one
Thiocarbohydrazide
Spirooctane-2',3-1,2,4,5-tetrahydro-s-tetrazine>-6-thione
Conditions | Yield |
---|---|
In ethanol for 24h; Substitution; | 70% |
bicyclo[3.2.1]octan-2-one
2,2-dihydroperoxybicyclo[3.2.1]octane
Conditions | Yield |
---|---|
Stage #1: bicyclo[3.2.1]octan-2-one With cross-linked poly(4-vinylpyridine):H2SO4 complex (1:5) In tetrahydrofuran at 0℃; for 0.0833333h; Stage #2: With cross-linked poly(4-vinylpyridine):H2O2 complex (1:4.5) In tetrahydrofuran at 0 - 20℃; for 24h; | 64% |
bicyclo[3.2.1]octan-2-one
dimethyl (methoxymethylene)malonate
4-Oxo-3-oxa-tricyclo[7.2.1.02,7]dodeca-2(7),5-diene-5-carboxylic acid methyl ester
Conditions | Yield |
---|---|
With lithium diisopropyl amide In tetrahydrofuran 1) -20 deg C 2) 3h -20 -> 25 deg C; | 62% |
With lithium diisopropyl amide 1.) THF, -78 to -5 deg C, 1.75 h 2.) THF, -30 to 25 deg C, 2.75 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With ethylenediamine for 24h; Heating; | 51% |
bicyclo[3.2.1]octan-2-one
methyltriphenylphosphonium iodide
2-methylenebicyclo<3.2.1>octane
Conditions | Yield |
---|---|
With n-butyllithium In diethyl ether | 44% |
bicyclo[3.2.1]octan-2-one
N-Cyanoguanidine
Conditions | Yield |
---|---|
at 200℃; for 1h; | 6.3% |
bicyclo[3.2.1]octan-2-one
bicyclo[3.2.1]octane-2,3,4-trione
Conditions | Yield |
---|---|
With selenium(IV) oxide |
bicyclo[3.2.1]octan-2-one
Bicyclo<3.2.1>octan-exo-2-ol
endo-bicyclo<3.2.1>-octan-2-ol
Conditions | Yield |
---|---|
With hydrogenchloride; acetic acid; platinum Hydrogenation; |
bicyclo[3.2.1]octan-2-one
endo-bicyclo<3.2.1>-octan-2-ol
Conditions | Yield |
---|---|
With methanol; ammonia; lithium weiteres Reagens: Aether; | |
With ammonia; lithium | |
(i) H2, PtO2, AcOH, aq. HCl, (ii) LiAlH4; Multistep reaction; |
chloraminophenamide
bicyclo[3.2.1]octan-2-one
6-chloro-1,1-dioxo-1,4-dihydro-2H-1λ6-spiro[benzo[1,2,4]thiadiazine-3,2'-bicyclo[3.2.1]octane]-7-sulfonic acid amide
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In 1,4-dioxane for 30h; Heating; |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate Irradiation; |
methyl magnesium iodide
bicyclo[3.2.1]octan-2-one
2-methylbicyclo<3.2.1>oct-2-ene
Conditions | Yield |
---|---|
(i) Et2O, (ii) I2; Multistep reaction; |
methyl magnesium iodide
bicyclo[3.2.1]octan-2-one
endo-2-Methyl-bicyclo<3.2.1>octan-exo-2-ol
cis-2-Methyl-bicyclo<3.2.1>octan-ol-(2)
Conditions | Yield |
---|---|
In diethyl ether |
tert-Butyl chloroacetate
bicyclo[3.2.1]octan-2-one
bicyclo[3.2.1]octane-2-carbaldehyde
Conditions | Yield |
---|---|
(i) KOtBu, (ii) (pyrolysis); Multistep reaction; |
Conditions | Yield |
---|---|
In tetrahydrofuran; water Irradiation; |
Conditions | Yield |
---|---|
(i) LDA, THF, (ii) (PhSe)2, Br2, (iii) aq. H2O2, Py, CH2Cl2; Multistep reaction; |
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In methanol Irradiation; |
bicyclo[3.2.1]octan-2-one
Conditions | Yield |
---|---|
With sodium borodeuteride; deuteriated sodium hydroxide In deuteromethanol |
bicyclo[3.2.1]octan-2-one
2-amino-benzenethiol
3H-spiro[benzothiazole-2,2'-bicyclo[3.2.1]octane]
Conditions | Yield |
---|---|
In ethanol for 18h; Heating; |
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