Conditions | Yield |
---|---|
With air; acetic acid; 1N,3N,5N-trihydroxy-1,3,5-triazin-2,4,6[1H,3H,5H]-trione; cobalt(II) acetate; zirconyl acetate at 150℃; under 15200 Torr; for 6h; | 81% |
With sodium hydroxide; potassium permanganate In water for 2h; Heating; | 80% |
Stage #1: 1,2,3-trimethylbenzene With potassium permanganate; potassium hydroxide In water at 95℃; for 4.08333h; Reflux; Stage #2: With sulfuric acid In water at 45℃; for 2h; Reagent/catalyst; | 80.67% |
With nitric acid |
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With potassium permanganate In water at 20℃; for 18h; | 42% |
Conditions | Yield |
---|---|
Reaktion ueber mehrere Stufen; | |
Multi-step reaction with 2 steps 1: NaOH; water / man gibt eine konzentrierte Loesung von KMnO4 in Wasser hinzu 2: water; KMnO4 View Scheme |
Conditions | Yield |
---|---|
With potassium hydroxide; potassium permanganate |
Conditions | Yield |
---|---|
With potassium hydroxide; potassium permanganate |
3-methylphthalic acid
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With potassium permanganate |
Conditions | Yield |
---|---|
With potassium permanganate; water |
2-acetyl-6-methyl-benzoic acid
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With potassium permanganate; sodium carbonate Ansaeuern des Reaktionsgemisches mit Schwefelsaeure; |
dimethyl 3-cyanobenzene-1,2-dicarboxylate
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With sodium hydroxide |
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With potassium permanganate |
Conditions | Yield |
---|---|
With potassium hydroxide; potassium permanganate |
Conditions | Yield |
---|---|
With alkaline permanganate |
Conditions | Yield |
---|---|
With nitric acid | |
With potassium permanganate at 100℃; |
Hemimellitsaeure-dimethyl-(1,2)-aethyl-(3)-ester
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol |
Conditions | Yield |
---|---|
With sodium hydroxide; potassium permanganate In water Heating; |
Conditions | Yield |
---|---|
With potassium permanganate In sodium hydroxide Heating; overnight; |
3-methyl-9-hydroxyphenalen-1-one
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With sodium hydroxide; potassium permanganate In water Heating; |
C17H16O2
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With potassium permanganate; sodium carbonate In water |
2,4-dibromo-naphthalene-1,8-dicarboxylic acid
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With sodium hydroxide; potassium permanganate |
isoquinoline-5-carboxylic acid
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
at 100℃; in neutraler Loesung; |
6-hydroxy-7-oxo-cyclohepta-1,3,5-triene-1,2-dicarboxylic acid-anhydride
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
at 180℃; |
acenaphthene
A
carbon dioxide
B
benzene-1,2,3-tricarboxlic acid
C
acide 2,6-carboxyphenylglyoxalique
D
oxalic acid
1,1-dimethyl-3-oxo-phthalan-4,5-dicarboxylic acid
A
benzene-1,2,3-tricarboxlic acid
B
acetone
acenaphthene quinone
A
Naphthalene-1,8-dicarboxylic acid
B
benzene-1,2,3-tricarboxlic acid
C
acide 2,6-carboxyphenylglyoxalique
1,1,4-trimethylcycloheptane
A
terephthalic acid
B
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
at 390 - 400℃; anschliessende Oxydation mit KMnO4 in wss.-alkal. Loesung; |
1,6-dimethylnaphthalene
A
carbon dioxide
B
benzene-1,2,3-tricarboxlic acid
C
oxalic acid
D
acetic acid
Conditions | Yield |
---|---|
In tetrahydrofuran at 150℃; for 6h; | 99% |
at 190 - 200℃; | |
at 150℃; for 12h; |
4,4'-bipyridine
benzene-1,2,3-tricarboxlic acid
water
sodium hydroxide
Conditions | Yield |
---|---|
In water High Pressure; Cu:acid:4,4'-bipy:NaOH=1:1:0.5:4, heated in autoclave at 170°C for 3 d; crysts. separated manually, washed (water, ethanol); elem. anal.; | A 95% B 2% |
Conditions | Yield |
---|---|
With sulfuric acid In methanol for 24h; Reflux; | 94% |
benzene-1,2,3-tricarboxlic acid
Tri-K-Salz von Hemimellitsaeure
Conditions | Yield |
---|---|
With potassium hydroxide In isopropyl alcohol | 88% |
benzene-1,2,3-tricarboxlic acid
water
cadmium(II) acetate dihydrate
N,N’-di(3-pyridyl)adipoamide
Conditions | Yield |
---|---|
at 120℃; for 48h; Autoclave; High pressure; | 86% |
Conditions | Yield |
---|---|
With Et3N In water High Pressure; mixt. of Co salt, C6H3(COOH)3, Et3N, (C5H4N)2C3H6 and H2O treated in autoclave at 175°C for 60 h; cooled to room temp. at a rate of 5°C/h; elem. anal., detd. by TGA; | 85% |
benzene-1,2,3-tricarboxlic acid
1,4-bis(imidazol-l-yl-methyl)benzene
water
Conditions | Yield |
---|---|
With sodium hydroxide at 160℃; for 72h; Autoclave; High pressure; | 66% |
Conditions | Yield |
---|---|
With NaOH In water High Pressure; Cu:acid:4,4'-bipy:NaOH=1:1:0.5:2, heated in autoclave at 170°C for 3 d; crysts. washed (water, ethanol); elem. anal.; | 65% |
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
In water High Pressure; mixt. Cu(NO3)2*3H2O, benzene-1,2,3-tricarboxylic acid and water was stirred at room temp. for 30 min and heated in Teflon-lined stainless-steel autoclave at 170°C for 50 h; react. mixt. was cooled to room temp. at 10°C/h, ppt. was filtered, washed with water and dried in air; elem. anal.; | 65% |
benzene-1,2,3-tricarboxlic acid
Conditions | Yield |
---|---|
With KOH In methanol; water soln. of (C6H3)(COOH)3 (1 mmol) in MeOH stirred with aq. KOH (3 mmol); aq. soln. of TlNO3 (3 mmol) added; refluxed (1 h); filtered; evapd. (several d); washed with acetone; dried in air; elem. anal.; | 65% |
benzene-1,2,3-tricarboxlic acid
zinc(II) acetate dihydrate
N,N′-bis(3-pyridyl)succinamide
Conditions | Yield |
---|---|
With sodium hydroxide at 120℃; for 48h; High pressure; | 65% |
1,10-Phenanthroline
benzene-1,2,3-tricarboxlic acid
zinc(II) acetate dihydrate
Conditions | Yield |
---|---|
In water at 120℃; for 72h; Temperature; Autoclave; | 65% |
Conditions | Yield |
---|---|
With sodium hydroxide at 140℃; for 72h; pH=7; Sealed tube; | 62% |
Conditions | Yield |
---|---|
With KOH In water High Pressure; pyrazine was added to aq. soln. of AgNO3 and 1,2,3-benzenetricarboxylic acid; pH was adjusted to 7.0 with dropwise addition of dilute KOH; placed in Teflon-lined stainless steel vessel; heated at 120°C for 3 ds; slowly cooled to room temp.; crystals were obtained; elem. anal.; | 61% |
Conditions | Yield |
---|---|
In water High Pressure; mixt. Cd(OH)2, benzene-1,2,3-tricarboxylic acid and water was stirred atroom temp. for 30 min and heated in Teflon-lined stainless-steel autocl ave at 170°C for 3 d; react. mixt. was cooled to room temp. at 8°C/h, ppt. was filtered, washed with water and dried in air; elem. anal.; | 60% |
Conditions | Yield |
---|---|
With Nd(NO3)3*6H2O In water aq. soln. of Ag compd.(0.25 mmol), ligand (0.33 mmol), and Nd compd. (0.125 mmol) refluxed for 2 h; cooled, filtered, crystd. on storage for 2 wk, elem. anal.; | 60% |
benzene-1,2,3-tricarboxlic acid
zinc(II) acetate dihydrate
N,N′-bis(3-pyridyl)succinamide
Conditions | Yield |
---|---|
With sodium hydroxide In water at 120℃; for 48h; Autoclave; | 60% |
benzene-1,2,3-tricarboxlic acid
1,4-bis(imidazol-l-yl-methyl)benzene
Conditions | Yield |
---|---|
With LiOH*H2O In water High Pressure; soln. of Zn(NO3)2*6H2O (0.1 mmol), H3BTC (0.1 mmol), bix (0.1 mmol) and LiOH*H2O (0.3 mmol) heated in Teflon-lined stainless steel autoclave at 140°C for 3 d; filtered, washed (H2O and EtOH); elem. anal.; | 58% |
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