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Cas:765-09-3
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Min.Order:5 Kiloliter
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Type:Manufacturers
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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inquiry1-Bromotridecane CAS:765-09-3 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermedia
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Min.Order:1 Gram
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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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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1-Bromotridecane cas 765-09-3Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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Conditions | Yield |
---|---|
With bromine; mercury(II) oxide In tetrachloromethane for 1.5h; Heating; | 92% |
With [bis(acetoxy)iodo]benzene; bromine In various solvent(s) for 22h; bromodecarboxylation; Heating; irradiation; | 79% |
(i) TlOEt, (ii) Br2; Multistep reaction; | |
With bromine; thallium (I) ethoxide 1.) hexane, 2.) reflux, 3 h; Yield given. Multistep reaction; | |
Multi-step reaction with 2 steps 1: oxalyl dichloride; N,N-dimethyl-formamide 2: dmap; Bromotrichloromethane; 2-mercaptopyridine-1-oxide sodium salt / 4 h / Reflux View Scheme |
Conditions | Yield |
---|---|
With carbon tetrabromide In dichloromethane at -30 - 20℃; | 88% |
With hydrogen bromide at 100℃; | |
With hydrogen bromide |
formaldehyde ditridecylacetal
1-bromotridecane
Conditions | Yield |
---|---|
With phosphorus pentabromide; benzene |
Conditions | Yield |
---|---|
With hydrogen bromide; dihydrogen peroxide |
1-bromotridecane
Conditions | Yield |
---|---|
With phosphorus pentabromide |
Conditions | Yield |
---|---|
in Gegenwart von Peroxyden; |
formaldehyde ditridecylacetal
phosphorus pentabromide
benzene
1-bromotridecane
1-bromotridecane
Conditions | Yield |
---|---|
With tetrachloromethane; bromine |
1-bromotridecane
Conditions | Yield |
---|---|
With bromine | |
With tetrachloromethane; bromine | |
With bromine |
1-bromotridecane
Conditions | Yield |
---|---|
With Trichloroethylene; bromine |
Conditions | Yield |
---|---|
With dmap; Bromotrichloromethane; 2-mercaptopyridine-1-oxide sodium salt for 4h; Hunsdiecker-Borodin reaction; Reflux; |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: dichloromethane / 20 °C 2: 10% Pd/C; hydrogen / ethanol / 20 °C 3: lithium aluminium tetrahydride / diethyl ether / 0 - 20 °C 4: carbon tetrabromide / dichloromethane / -30 - 20 °C View Scheme |
(E)-Tridec-2-enoic acid ethyl ester
1-bromotridecane
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 10% Pd/C; hydrogen / ethanol / 20 °C 2: lithium aluminium tetrahydride / diethyl ether / 0 - 20 °C 3: carbon tetrabromide / dichloromethane / -30 - 20 °C View Scheme |
ethyl tridecanoate
1-bromotridecane
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / diethyl ether / 0 - 20 °C 2: carbon tetrabromide / dichloromethane / -30 - 20 °C View Scheme |
1-bromotridecane
3-(tetrahydropyran-2'-yloxy)propyne
2-(hexadec-2-yn-1-yloxy)tetrahydro-2H-pyran
Conditions | Yield |
---|---|
With n-butyllithium at -30℃; for 1h; | 100% |
Stage #1: 3-(tetrahydropyran-2'-yloxy)propyne With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; n-butyllithium In tetrahydrofuran at -78℃; for 1.5h; Stage #2: 1-bromotridecane In tetrahydrofuran at 20℃; for 21h; | 76% |
Stage #1: 3-(tetrahydropyran-2'-yloxy)propyne With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: 1-bromotridecane With N,N,N,N,N,N-hexamethylphosphoric triamide In tetrahydrofuran; hexane at -78℃; for 24h; | 60% |
With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium 1.) THF; Multistep reaction; | |
Stage #1: 3-(tetrahydropyran-2'-yloxy)propyne With n-butyllithium In tetrahydrofuran; hexane at 0℃; Stage #2: 1-bromotridecane In tetrahydrofuran; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; hexane at 40℃; for 24h; |
Conditions | Yield |
---|---|
In ethanol for 18h; Reflux; | 100% |
In ethanol for 12h; Reflux; |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 50℃; | 100% |
4-amino-1-benzylpiperidine
1-bromotridecane
Conditions | Yield |
---|---|
With triethylamine In acetonitrile for 3h; Heating; | 99% |
1-bromotridecane
N,N-bis[3-(dimethylamino)propyl]-N',N'-dimethylpropane-1,3-diamine
Conditions | Yield |
---|---|
In acetonitrile for 24h; Reflux; | 99% |
1-bromotridecane
Conditions | Yield |
---|---|
Stage #1: 2,4-di-(azetidin-1-yl)-6-methylpyrimidine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1.25h; Inert atmosphere; Stage #2: 1-bromotridecane In tetrahydrofuran; hexane at 0℃; for 1h; Inert atmosphere; | 98% |
Stage #1: 2,4-di-(azetidin-1-yl)-6-methylpyrimidine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere; Stage #2: 1-bromotridecane In tetrahydrofuran; hexane at -78 - 0℃; for 1h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With ethylenediamine In dimethyl sulfoxide at 0 - 20℃; | 97.9% |
In dimethyl sulfoxide at 20℃; for 1h; | 91% |
1-bromotridecane
methyl 4'-hydroxy-4-biphenylcarboxylate
4'-tridecyloxy-biphenyl-4-carboxylic acid methyl ester
Conditions | Yield |
---|---|
Stage #1: methyl 4'-hydroxy-4-biphenylcarboxylate With potassium carbonate; caesium carbonate In acetone for 0.0833333h; Inert atmosphere; Stage #2: 1-bromotridecane In acetone for 72h; Inert atmosphere; Reflux; | 97.3% |
Conditions | Yield |
---|---|
Stage #1: diphenyl diselenide With sodium tetrahydroborate In tetrahydrofuran; ethanol Reduction; Stage #2: 1-bromotridecane In tetrahydrofuran; ethanol at 60℃; Substitution; | 97% |
1-bromotridecane
2-ethoxycarbonyl-1-cyclopentanone
ethyl 2-oxo-1-n-tridecylcyclopentanecarboxylate
Conditions | Yield |
---|---|
Stage #1: 2-ethoxycarbonyl-1-cyclopentanone With potassium carbonate; potassium iodide In acetone for 0.166667h; Stage #2: 1-bromotridecane In acetone at 62℃; for 20h; | 97% |
3-(3,4-trihydroxyphenyl)propionic acid methyl ester
1-bromotridecane
3-(3,4,5-tris-tridecyloxyphenyl)propionic acid methyl ester
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 75℃; for 8h; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 96% |
1-bromotridecane
5-amino-3-mercapto-4H-[1,2,4]triazole
5-Tridecylsulfanyl-4H-[1,2,4]triazol-3-ylamine
Conditions | Yield |
---|---|
With triethylamine In acetonitrile for 2h; Heating; | 95% |
1-bromotridecane
bis(p-chlorophenyl) diselenide
Conditions | Yield |
---|---|
Stage #1: bis(p-chlorophenyl) diselenide With sodium tetrahydroborate In tetrahydrofuran; ethanol Reduction; Stage #2: 1-bromotridecane In tetrahydrofuran; ethanol at 60℃; Substitution; | 95% |
1-bromotridecane
Conditions | Yield |
---|---|
Stage #1: 4-(azetidin-1-yl)-2-cyclobutanoxy-6-methylpyrimidine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1.25h; Inert atmosphere; Stage #2: 1-bromotridecane In tetrahydrofuran; hexane at 0℃; for 1h; Inert atmosphere; | 95% |
Stage #1: 4-(azetidin-1-yl)-2-cyclobutanoxy-6-methylpyrimidine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere; Stage #2: 1-bromotridecane In tetrahydrofuran; hexane at -78 - 0℃; for 1h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
In acetonitrile Reflux; | 93% |
In acetonitrile Reflux; | 93% |
1-bromotridecane
(2S,3S)-3,4-epoxy-1,2-di-O-isopropylidenebutane-1,2-diol
(S)-1-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)pentadecan-1-ol
Conditions | Yield |
---|---|
Stage #1: 1-bromotridecane With magnesium In tetrahydrofuran Stage #2: With copper(l) cyanide In tetrahydrofuran at -20℃; for 0.5h; Stage #3: (2S,3S)-3,4-epoxy-1,2-di-O-isopropylidenebutane-1,2-diol regioselective reaction; Further stages; | 92% |
1-bromotridecane
(1R,2R)-1,2-bis((S)-2,2-dimethyl-1,3-dioxolan-4-yl)ethane-1,2-diol
Conditions | Yield |
---|---|
Stage #1: (1R,2R)-1,2-bis((S)-2,2-dimethyl-1,3-dioxolan-4-yl)ethane-1,2-diol With sodium hydride In N,N-dimethyl-formamide for 0.5h; Cooling with ice; Stage #2: 1-bromotridecane In N,N-dimethyl-formamide at 20℃; for 4h; | 92% |
1-bromotridecane
Conditions | Yield |
---|---|
Stage #1: 2,4-dicyclobutanoxy-6-methylpyrimidine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1.25h; Inert atmosphere; Stage #2: 1-bromotridecane In tetrahydrofuran; hexane at 0℃; for 1h; Inert atmosphere; | 92% |
Stage #1: 2,4-dicyclobutanoxy-6-methylpyrimidine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere; Stage #2: 1-bromotridecane In tetrahydrofuran; hexane at -78 - 0℃; for 1h; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
With sodium hydride In water at 66℃; for 12h; Temperature; Solvent; Cooling with ice; | 91.1% |
Conditions | Yield |
---|---|
Stage #1: 6-mercapto-1-hexanol With 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide at 20℃; for 0.333333h; Stage #2: 1-bromotridecane In N,N-dimethyl-formamide at 65℃; for 3h; | 91% |
1-bromotridecane
triphenylphosphine
n-tridecyltriphenylphosphonium bromide
Conditions | Yield |
---|---|
In acetonitrile for 24h; Heating; | 90% |
In toluene for 26h; Inert atmosphere; Reflux; | 85% |
In toluene Reflux; | 85% |
Conditions | Yield |
---|---|
In acetonitrile Reflux; | 90% |
In acetonitrile Reflux; | 90% |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; potassium carbonate In N,N-dimethyl-formamide at 20℃; for 24h; | 89% |
Conditions | Yield |
---|---|
With potassium carbonate In tetrahydrofuran; N,N-dimethyl-formamide at 0 - 60℃; for 18h; | 88% |
With sodium hydride In tetrahydrofuran at 0 - 70℃; for 18.6667h; Inert atmosphere; | 75% |
(i) Na, (ii) /BRN= 1739992/; Multistep reaction; |
1-bromotridecane
tris(tert-butyldimethylsilyloxy)tris(methoxymethoxy)dehydrobenzo[12]annulene
Conditions | Yield |
---|---|
With cesium fluoride In N,N-dimethyl-formamide at 70℃; for 5.5h; Inert atmosphere; Schlenk technique; | 88% |
1-bromotridecane
(4R,5R)-5-benzyloxy-4-ethynyl-2,2-dimethyl-1,3-dioxane
(4R,5R)-5-benzyloxy-4-(pentadec-1-ynyl)-2,2-dimethyl-1,3-dioxane
Conditions | Yield |
---|---|
With n-butyllithium | 87% |
With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium In tetrahydrofuran; hexane at -78 - 20℃; for 10.5h; Alkylation; | 87% |
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