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inquiryProduct Name: 5-Dibenzosuberenone Synonyms: 5H-DIBENZO[A,D]CYCLOHEPTEN-5-ONE;5H-DIBENZO(A,D)CYCLOHEPTENE-5-OL;5-DIBENZOSUBERENONE;DIBENZOSUBERENONE;DIBENZOSUBERENONE-5;DIBENZO[A,D]-CYCLOHEPTEN
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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inquiryDibenzosuberenoneAppearance:White or Almost White crystalline powder Storage:Store in refrigerator Package:according to customers' requirements Application:Steroids injection For Body building Transportation:By air(EMS or EUB or FedEx or TNT ect...)
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inquiry5-Dibenzosuberenone Basic information Product Name: 5-Dibenzosuberenone Synonyms: Cyproheptadine Impurity B;Cyproheptadine impurity B (5h-dibenzo A, D cycloheptene-5-one);5H-DIBENZO[A,D]CYCLOHEPTEN-5-ONE;5H-DIBENZO(A,D)CYCLOHEPTENE-5-OL;5-DIBE
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inquiryWuhan Xinweiye Chemical Co., Ltd. is mainly engaged in the process development and production of customized synthesis and pharmaceutical intermediates. We have professional researchers in organic synthesis, analytical chemistry and production process
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Shanghai Lonwin Chemical company is a subsidiary of Lonwin Industry Group Limited, was established in 2011 and is headquartered in Shanghai, adjacent to China National Convention and Exhibition Center and Hongqiao transportation hub.Lonwinchem is
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inquirytrans-10,11-dibromo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one
dibenzosuberenon
Conditions | Yield |
---|---|
With sodium selenite; rac-cysteine In tetrahydrofuran; water at 0℃; for 0.0833333h; | 99% |
With dimethyl sulfoxide at 75℃; for 2h; | 98% |
With hydrogenchloride; samarium In tetrahydrofuran for 0.166667h; Ambient temperature; | 96% |
10,11-dibromo[(10,11-dihydro-5H-dibenzo[a,d]cyclohept-5-one)]
dibenzosuberenon
Conditions | Yield |
---|---|
With N,N,N,N,-tetramethylethylenediamine; sexithiophene In N,N-dimethyl-formamide for 1h; Inert atmosphere; Irradiation; | 99% |
With sodium hydride; 2,8,9-trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane hydro-chloride In [D3]acetonitrile for 2h; | 92% |
5H-dibenzo[a,d]cyclohepten-5-ol
dibenzosuberenon
Conditions | Yield |
---|---|
With Merrifield's resin-bound N-aminoimidazolium chlorochromate In dichloromethane for 2.5h; Heating; | 95% |
With tert.-butylhydroperoxide In water at 100℃; for 24h; | 91% |
Stage #1: 5H-dibenzo[a,d]cyclohepten-5-ol With 7,7-dichlorocyclohepta-1,3,5-triene In dichloromethane; dimethyl sulfoxide at -30℃; for 0.333333h; Swern Oxidation; Inert atmosphere; Stage #2: With triethylamine In dichloromethane; dimethyl sulfoxide at -30 - 20℃; for 0.333333h; Swern Oxidation; Inert atmosphere; | 88% |
trans-10,11-dibromodibenzosuberenone
dibenzosuberenon
Conditions | Yield |
---|---|
With indium; niobium pentachloride In tetrahydrofuran at 20℃; for 0.166667h; Sonication; chemoselective reaction; | 95% |
With indium; cobalt(II) chloride hexahydrate In methanol at 20℃; for 1h; | 94% |
With gallium; bis(cyclopentadienyl)titanium dichloride In tetrahydrofuran at 20℃; for 0.416667h; Inert atmosphere; Ultrasonic irradiation; chemoselective reaction; | 92% |
Conditions | Yield |
---|---|
With dimethylboron bromide In dichloromethane; 1,2-dichloro-ethane at -78℃; for 1h; | 93% |
With dimethylboron bromide; sodium hydrogencarbonate 1) CH2Cl2, -78 deg C, 1h, 2) THF, 5 min; Yield given. Multistep reaction; |
5-(3,3-diphenyl-2,3-dihydro-2-oxoindol-1-yl)dibenzocyclohepten-1-yl diphenylethanoate
dibenzosuberenon
Conditions | Yield |
---|---|
With hydrogenchloride; water In acetic acid for 1h; Heating; | 83% |
Conditions | Yield |
---|---|
With indium; indium chloride In water; tert-butyl alcohol at 84℃; for 6h; | 81% |
5-Allyl-dibenzo-cyclohepten-5-ol
B
9.18-Dioxo-4b.4c.9.13b.13c.18-hexahydro-tetrabenzocyclobutadicyclohepten
C
dibenzosuberenon
Conditions | Yield |
---|---|
In ethyl acetate at 20℃; for 2h; Inert atmosphere; Photolysis; | A 81% B 6% C 8% |
5-phenyl-5H-dibenzocyclohepten-5-ol
dibenzosuberenon
Conditions | Yield |
---|---|
With sulfuric acid; dihydrogen peroxide; acetic acid for 4h; Ambient temperature; | 79% |
5-<(5H-dibenzocyclohepten-5-yl)oxy>-5H-dibenzocycloheptene
A
suberene
B
dibenzosuberenon
Conditions | Yield |
---|---|
With iodine In neat (no solvent) at 85℃; | A 73% B 79% |
Conditions | Yield |
---|---|
With bromine at 140℃; | 70% |
With tetrachloromethane; N-Bromosuccinimide; dibenzoyl peroxide Erhitzen des Reaktionsprodukts mit Triaethylamin; | |
With tetrachloromethane; N-Bromosuccinimide; dibenzoyl peroxide Erhitzen des Reaktionsprodukts mit Pyridin; |
Conditions | Yield |
---|---|
In ethyl acetate at 20℃; for 2h; Inert atmosphere; Photolysis; | A 68% B 25% |
5-(3,3-dimethyl-2,3-dihydro-2-oxoindol-1-yl)dibenzocyclohepten-1-yl 2-methylpropanoate
dibenzosuberenon
Conditions | Yield |
---|---|
With hydrogenchloride; water In acetic acid for 0.5h; Heating; | 51% |
A
9.18-Dioxo-4b.4c.9.13b.13c.18-hexahydro-tetrabenzocyclobutadicyclohepten
B
dibenzosuberenon
Conditions | Yield |
---|---|
In ethyl acetate at 20℃; for 2h; Solvent; Inert atmosphere; Photolysis; | A 12% B 50% |
dibenzosuberol
A
suberene
B
anthracene
C
9-methylanthracene
D
dibenzosuberenon
Conditions | Yield |
---|---|
With quartz at 350 - 650℃; Inert atmosphere; Pyrolysis; | A 20% B 15% C 12% D 40% |
A
5,5'-bi(5H-dibenzocycloheptenyl)
C
9.18-Dioxo-4b.4c.9.13b.13c.18-hexahydro-tetrabenzocyclobutadicyclohepten
D
dibenzosuberenon
Conditions | Yield |
---|---|
In ethyl acetate at 20℃; for 2h; Solvent; Inert atmosphere; Photolysis; | A 8% B 6% C 22% D 39% |
In ethyl acetate at 20℃; for 2h; Inert atmosphere; Photolysis; | A 14% B 8% C 38% D 20% |
5-diazo-5H-dibenzocycloheptene
A
suberene
B
4H-Cyclopenta[def]phenanthrene
C
dibenzosuberenon
Conditions | Yield |
---|---|
at 450℃; under 1E-05 Torr; | A n/a B 17% C n/a |
at 450℃; under 1E-05 Torr; Mechanism; | A n/a B 17% C n/a |
Conditions | Yield |
---|---|
With 1,4-dioxane; selenium(IV) oxide |
dibenzosuberenon
Conditions | Yield |
---|---|
With aluminium trichloride |
methanol
5-diazo-5H-dibenzocycloheptene
A
5-methoxy-5H-dibenzocycloheptene
B
5,5-dimethoxy-5H-dibenzocycloheptene
C
dibenzosuberenon
Conditions | Yield |
---|---|
at 60℃; electrooxidation; | A 56.6 % Spectr. B 30.2 % Spectr. C 7.1 % Spectr. |
at 60℃; electrooxidation; | A n/a B 30.2 % Spectr. C n/a |
methanol
C15H10N2(1+)
A
5-methoxy-5H-dibenzocycloheptene
B
5,5-dimethoxy-5H-dibenzocycloheptene
C
dibenzosuberenon
Conditions | Yield |
---|---|
With tetramethylammonium tetrafluoroborate In acetonitrile at 0 - 50℃; Kinetics; Thermodynamic data; electrolyte effect, substrate concentration, effect of solvent, deuterated solvent (in methanol), ΔH(excit.), ΔS(excit.); |
5-diazo-5H-dibenzocycloheptene
A
5-methoxy-5H-dibenzocycloheptene
B
5,5-dimethoxy-5H-dibenzocycloheptene
C
dibenzosuberenon
Conditions | Yield |
---|---|
In methanol at 60℃; electrooxidation; | A 56.6 % Spectr. B 30.2 % Spectr. C 7.1 % Spectr. |
dibenzosuberenon
Conditions | Yield |
---|---|
With 1,5-diselenacyclooctane In chloroform at 90℃; for 95h; | 28 % Chromat. |
5H-6,7-dihydrodibenzo[a,c]cyclohepten-6-ol
A
suberene
B
anthracene
C
9-methylanthracene
D
dibenzosuberenon
Conditions | Yield |
---|---|
at 350℃; under 997.58 Torr; Product distribution; Further Variations:; Temperatures; other dibenzocycloalkanols; | A 15 % Spectr. B 4 % Spectr. C 4 % Spectr. D 20 % Spectr. |
dibenzosuberane
A
10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-one
B
dibenzosuberenon
Conditions | Yield |
---|---|
With aluminum oxide; Ru(OH)x; oxygen In 1,2-dichloro-benzene at 169.85℃; under 760 Torr; for 5h; |
5H-dibenzocyclohepten-5-one hydrazone
dibenzosuberenon
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.) sodium sulphate, yellow mercuric oxide, potassium hydroxide, Celite / 1.) diethyl ether, ethanol, 3 h, 2.) ethanol, diethyl ether, room temp., overnight 2: 82 percent / benzene / 8 h / Ambient temperature 3: 83 percent / water, hydrochloric acid / acetic acid / 1 h / Heating View Scheme |
dibenzocyclohepten-5-ylidene(phenyl)amine N-oxide
dibenzosuberenon
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 82 percent / benzene / 8 h / Ambient temperature 2: 83 percent / water, hydrochloric acid / acetic acid / 1 h / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: polyphosphoric acid 2: bromine / Irradiation View Scheme |
diphenylethane-2-carboxylic acid chloride
dibenzosuberenon
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AlCl3; CS2 2: N-bromo-succinimide; CCl4; dibenzoyl peroxide / Erhitzen des Reaktionsprodukts mit Triaethylamin View Scheme |
Conditions | Yield |
---|---|
With iodine; hypophosphorous acid In acetic acid for 72h; Reduction; Heating; | 100% |
With potassium hydroxide; Raney Ni-Al alloy In water at 90℃; for 8h; | 92% |
With ethanol; platinum Hydrogenation; | |
With ethanol; sodium |
Conditions | Yield |
---|---|
With titanium tetrachloride In toluene at -10 - 20℃; Inert atmosphere; | 100% |
With titanium tetrachloride In benzene for 144h; Ambient temperature; | 95% |
With titanium tetrachloride In toluene |
dibenzosuberenon
N-[tricyclo[9.4.0.03,8]pentadeca-1(11),3,5,7,9,12,14-heptaen-2-ylidene]hydroxylamine
Conditions | Yield |
---|---|
With hydroxylamine hydrochloride In pyridine for 20h; Reflux; Inert atmosphere; | 100% |
With pyridine; hydroxylamine hydrochloride for 15.5h; Reflux; | 100% |
With pyridine; hydroxylamine hydrochloride In ethanol Reflux; | 98% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; aluminium trichloride In tetrahydrofuran; diethyl ether | 99% |
With lithium aluminium tetrahydride; aluminium trichloride In diethyl ether | 65% |
With aluminum isopropoxide at 250℃; for 0.166667h; | 50% |
With potassium hydroxide; hydrazine hydrate; isopropyl alcohol Reagens 4: Propan-1,3-dion; Abdestillieren des Loesungsmittels und Erhitzen auf 200grad; | |
With lithium aluminium tetrahydride; aluminium trichloride In tetrahydrofuran; diethyl ether for 2h; Heating; Yield given; |
4-chloro-1-methylpiperidine
dibenzosuberenon
5-(1-methyl-4-piperidyl)-5H-dibenzocyclohepten-5-ol
Conditions | Yield |
---|---|
Stage #1: 4-chloro-1-methylpiperidine With iodine; magnesium In tetrahydrofuran for 5h; Reflux; Inert atmosphere; Stage #2: With (trimethylsilyl)methylmagnesium chloride; lithium chloride; zinc(II) chloride In tetrahydrofuran; diethyl ether at 20℃; for 0.75h; Inert atmosphere; Stage #3: dibenzosuberenon In tetrahydrofuran; diethyl ether at 0℃; for 2h; Inert atmosphere; | 99% |
Stage #1: 4-chloro-1-methylpiperidine With magnesium In tetrahydrofuran at 60 - 65℃; for 1h; Inert atmosphere; Large scale; Stage #2: dibenzosuberenon In tetrahydrofuran at 5 - 20℃; for 1h; Temperature; Inert atmosphere; Large scale; |
Conditions | Yield |
---|---|
With hydrogenchloride; potassium permanganate In water; acetone at 20℃; for 24h; | 99% |
dibenzosuberenon
5H-dibenzo[a,d]cyclohepten-5-ol
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate In methanol; water | 98% |
With sodium borohydrid In diethyl ether; water | 98% |
With sodium borohydrid In diethyl ether; water | 98% |
dibenzosuberenon
dibenzocyclohepten-5-imine
Conditions | Yield |
---|---|
With 1,1,1,3,3,3-hexamethyl-disilazane; scandium tris(trifluoromethanesulfonate) In chlorobenzene at 90℃; for 12h; Inert atmosphere; | 98% |
With ammonia; titanium tetrachloride In toluene at 25℃; for 16h; | 93% |
With ammonia; titanium tetrachloride In toluene at 0 - 25℃; for 12.25h; | 80.4% |
With ammonia; titanium tetrachloride In toluene at 25℃; overnight; | 20.6 g |
With ammonia; titanium tetrachloride In toluene |
Conditions | Yield |
---|---|
Stage #1: bromobenzene With magnesium In tetrahydrofuran for 0.333333h; Stage #2: dibenzosuberenon In tetrahydrofuran for 0.5h; Heating; | 97% |
With magnesium 1) Et2O, 2) Et2O, 2a) reflux, 2 h, 2b) r. t., 2 h; Yield given. Multistep reaction; |
methylmagnesium bromide
dibenzosuberenon
5-hydroxy-5-methyl-5H-dibenzocycloheptene
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether Ambient temperature; | 97% |
In tetrahydrofuran; diethyl ether at 15 - 20℃; for 2h; | 83% |
In diethyl ether for 1h; Heating; | 71% |
2-(phenylethynyl)phenylacetylene
dibenzosuberenon
5-[[2-(phenylethynyl)phenyl]ethynyl]-5H-dibenzo[a,d]cyclohepten-5-ol
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran at 0 - 20℃; for 2.5h; | 97% |
Conditions | Yield |
---|---|
Stage #1: 2-Bromobiphenyl; dibenzosuberenon With n-butyllithium In tetrahydrofuran at -78 - 20℃; Stage #2: With hydrogenchloride; acetic acid In water for 0.333333h; Heating; | 97% |
Stage #1: 2-Bromobiphenyl With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: dibenzosuberenon In tetrahydrofuran; hexane for 6h; Stage #3: With hydrogenchloride; acetic acid In water for 12h; Reflux; | 94% |
Stage #1: 2-Bromobiphenyl; dibenzosuberenon With tert.-butyl lithium In tetrahydrofuran; hexane at -78℃; for 6.5h; Stage #2: With hydrogenchloride; acetic acid In water for 12h; Reflux; | 94% |
Stage #1: 2-Bromobiphenyl In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: dibenzosuberenon In tetrahydrofuran; hexane for 6h; Stage #3: With hydrogenchloride; acetic acid In water for 12h; Reflux; | 94% |
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane -78 deg C to rt; | 96% |
Conditions | Yield |
---|---|
In toluene at 120℃; for 10h; Diels-Alder Cycloaddition; Sealed tube; | 96% |
In toluene at 120℃; for 20h; Diels-Alder Cycloaddition; | 94% |
3,6-di(pyridin-4-yl)-1,2,4,5-tetrazine
dibenzosuberenon
Conditions | Yield |
---|---|
In toluene at 125℃; for 16h; Diels-Alder Cycloaddition; Sealed tube; | 96% |
dibenzosuberenon
trans-10,11-dibromo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one
Conditions | Yield |
---|---|
With bromine In tetrachloromethane | 95% |
With bromine In tetrachloromethane for 1.5h; | 90% |
With bromine In chloroform at 0 - 20℃; Inert atmosphere; | 74% |
dibenzosuberenon
10,11-dibromo[(10,11-dihydro-5H-dibenzo[a,d]cyclohept-5-one)]
Conditions | Yield |
---|---|
With bromine In tetrachloromethane for 5.25h; | 95% |
With bromine In tetrachloromethane at 20℃; for 1.5h; | 92% |
With bromine In tetrachloromethane at 20℃; for 1.5h; | 92% |
With bromine In acetic acid |
dibenzosuberenon
N-methyl-5H-dibenzocyclohepten-5-imine
Conditions | Yield |
---|---|
With methylamine; titanium tetrachloride In benzene | 95% |
dibenzosuberenon
allylmagnesium bromide
5-Allyl-dibenzo-cyclohepten-5-ol
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; | 95% |
dibenzosuberenon
Conditions | Yield |
---|---|
With pyridine; [15N]hydroxylamine hydrochloride for 16h; Reflux; | 95% |
Conditions | Yield |
---|---|
In toluene at 120℃; for 8h; Diels-Alder Cycloaddition; | 95% |
In toluene at 100℃; for 10h; Diels-Alder Cycloaddition; Sealed tube; | 95% |
1,2,4,5-tetrazine-3,6-dicarboxamide
dibenzosuberenon
Conditions | Yield |
---|---|
In neat (no solvent) at 100℃; for 16h; Diels-Alder Cycloaddition; Sealed tube; | 95% |
dibenzosuberenon
5H-dibenzocyclohepten-5-one hydrazone
Conditions | Yield |
---|---|
With hydrazine hydrochloride; hydrazine hydrate In various solvent(s) Heating; | 94% |
Multi-step reaction with 2 steps 1: Lawessons reagent / benzene / 24 h / Reflux 2: hydrazine hydrate / benzene; ethanol / 2 h / Reflux View Scheme |
isopropylmagnesium bromide
dibenzosuberenon
A
5H-dibenzo[a,d]cyclohepten-5-ol
B
5-isopropyl-5H-dibenzo[a,d]cyclohepten-5-ol
Conditions | Yield |
---|---|
Stage #1: isopropylmagnesium bromide With (trimethylsilyl)methylmagnesium chloride; lithium chloride; zinc(II) chloride In tetrahydrofuran; diethyl ether at 20℃; Grignard addition; Stage #2: dibenzosuberenon In tetrahydrofuran; diethyl ether at 0℃; for 3h; Grignard addition; | A 6% B 94% |
Stage #1: isopropylmagnesium bromide With (trimethylsilyl)methylmagnesium chloride; lithium chloride; zinc(II) chloride In tetrahydrofuran; diethyl ether at 20℃; for 0.75h; Inert atmosphere; Stage #2: dibenzosuberenon In tetrahydrofuran; diethyl ether at 0℃; for 3h; Inert atmosphere; | A 6% B 94% |
In tetrahydrofuran at 0℃; Grignard addition; | A 89% B 11% |
diethyl isocyanomethylphosphonate
dibenzosuberenon
Conditions | Yield |
---|---|
Stage #1: diethyl isocyanomethylphosphonate With n-butyllithium In tetrahydrofuran at -78℃; for 1h; Horner-Wadsworth-Emmons Olefination; Stage #2: dibenzosuberenon In tetrahydrofuran for 16h; Horner-Wadsworth-Emmons Olefination; | 94% |
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