Conditions | Yield |
---|---|
With potassium carbonate In acetone at 60℃; for 16h; | 100% |
With potassium carbonate; potassium iodide In acetonitrile at 95℃; for 3h; Inert atmosphere; | 98.1% |
With potassium carbonate In acetone at 20℃; for 15h; Heating; Reflux; | 97% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 90℃; for 12h; | 98% |
In N,N-dimethyl-formamide at 80℃; for 8h; | 70% |
In N,N-dimethyl-formamide at 80℃; for 28h; Inert atmosphere; | 48.9% |
In pyridine; methanol at 115℃; Rate constant; Product distribution; | |
In N,N-dimethyl-formamide at 90℃; for 0.25h; |
2,6-dibromo-4-methoxyaniline
3,5-dibromoanisole
Conditions | Yield |
---|---|
With sulfuric acid; hypophosphorous acid; sodium nitrite In toluene at 0℃; for 4.5h; | 96% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; | 95% |
In methanol; DMF (N,N-dimethyl-formamide) at 0 - 20℃; for 1h; | |
In N,N-dimethyl-formamide at 20℃; |
Conditions | Yield |
---|---|
With potassium hydroxide; tetrabutylammomium bromide In tetramethylurea at 20℃; for 24h; | 84% |
With tetrabutylammomium bromide; oxygen; potassium hydroxide In tetramethylurea at 20℃; | 84% |
With potassium hydroxide; tetrabutylammomium bromide; tetramethylurea at 20℃; for 24.25h; | 84% |
With potassium hydroxide; tetrabutylammomium bromide In tetramethylurea at 20℃; for 24.25h; | 84% |
1,3,5-trisbromobenzene
3,5-dibromoanisole
Conditions | Yield |
---|---|
With sodium methylate In N,N-dimethyl-formamide at 100℃; for 12h; | 83% |
1,3,5-trisbromobenzene
sodium methylate
A
3,5-dibromophenol
B
3,5-dibromoanisole
Conditions | Yield |
---|---|
at 130℃; | |
at 120 - 130℃; im geschlossenen Rohr; |
Conditions | Yield |
---|---|
With methanol; sodium at 120 - 130℃; im geschlossenen Rohr; |
2,4-dibromo-6-methoxyaniline
A
3-bromo-5-nitroanisole
B
3,5-dibromoanisole
Conditions | Yield |
---|---|
With potassium disulphite; nitric acid nachfolgend Verkochen mit Alkohol in Gegenwart von Kupfersulfat; | |
With potassium disulphite; nitric acid Diazotization.folgend Verkochen mit Alkohol in Gegenwart von Kupfersulfat; |
2,4-dibromo-6-methoxyaniline
3,5-dibromoanisole
Conditions | Yield |
---|---|
With ethanol Diazotization; | |
With ethanol; sulfuric acid; sodium nitrite 1.) 0 deg C, 2.) 0 deg C, 15 min, 3.) heating to 80 deg C, 1 h;; Yield given. Multistep reaction; | |
beim Diazotieren und Kochen des Diazoniumsalzes in Alkohol; |
Conditions | Yield |
---|---|
With sodium hydroxide | |
With potassium hydroxide | |
With aq. alkali |
Conditions | Yield |
---|---|
With aluminium trichloride; potassium carbonate 1.) benzene; Multistep reaction; |
2,4-dibromo-6-methoxyaniline
nitric acid
A
3-bromo-5-nitroanisole
B
3,5-dibromoanisole
Conditions | Yield |
---|---|
beim nachfolgenden Verkochen mit Alkohol in Gegenwart von Kupfersulfat.Diazotization; |
1,3,5-trisbromobenzene
sodium methylate
A
1,2,3-trimethoxybenzene
B
1-bromo-3,5-dimethoxybenzene
C
3,5-dibromoanisole
Conditions | Yield |
---|---|
With copper(I) chloride; air In N,N-dimethyl-formamide at 110℃; |
2-methoxy-phenylamine
3,5-dibromoanisole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: glacial acetic acid / beim Bromieren 2: beim Diazotieren und Kochen des Diazoniumsalzes in Alkohol View Scheme |
3,5-dibromoaniline
3,5-dibromoanisole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Diazotization.Verkochen der Diazoniumsulfatloesung mit Schwefelsaeure 2: NaOH-solution View Scheme |
3,5-dibromoanisole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: concentrated hydrochloric acid 2: potassium pyrosulfite; nitric acid / Diazotization.folgend Verkochen mit Alkohol in Gegenwart von Kupfersulfat View Scheme |
1,3-dibromo-5-fluorobenzene
3,5-dibromoanisole
Conditions | Yield |
---|---|
With sodium methylate In methanol; DMF (N,N-dimethyl-formamide) at 0 - 20℃; for 1h; | |
With sodium methylate In methanol; N,N-dimethyl-formamide |
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