Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 110℃; for 4h; Temperature; | 92.2% |
With sulfuric acid; nitric acid at 20 - 100℃; Nitration; | 89% |
With sulfuric acid; nitric acid 1.) 0 deg C, 10 min, 2.) 95 deg C, 6 h, then room temp., 12 h; | 69% |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 110℃; for 4h; | 92.2% |
With sulfuric acid; nitric acid | |
durch Nitrierung; |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 20 - 90℃; Nitration; | 84% |
With nitric acid; Petroleum ether azeotropes Abdestillieren des gebildeten Wassers; | |
With sulfuric acid; nitric acid |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid 1.) 90-100 deg C, 2 h, 2.) 25 deg C, overnight; | 62% |
Nitrierung; | |
durch Nitrierung; |
Conditions | Yield |
---|---|
With lead(IV) acetate; acetic acid |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 60 - 70℃; |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 93 - 103℃; | |
With ammonium nitrate In sulfuric acid at 0 - 25℃; |
2,4,6-trinitrophenylacetic acid
2,4,6-Trinitrotoluene
Conditions | Yield |
---|---|
With water | |
With ethanol |
meta-dinitrobenzene
lead(IV) tetraacetate
acetic acid
A
2,4,6-Trinitrotoluene
B
2,4-dimethyl-1,3,5-trinitrobenzene
Conditions | Yield |
---|---|
Erwaermen des Reaktionsprodukts mit rauchender Salpetersaeure und konz. H2SO4 auf 75-120grad; |
1,3,5-trinitrobenzene
lead(IV) tetraacetate
acetic acid
A
2,4,6-Trinitrotoluene
B
2,4-dimethyl-1,3,5-trinitrobenzene
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid Thermodynamic data; ΔH, E(a); |
2,4-dinitrotoluene
A
2,4,6-Trinitrotoluene
B
1-bromo-2-methyl-3,5-dinitrobenzene
Conditions | Yield |
---|---|
With sulfuric acid; bromine; nitric acid at 90℃; for 0.166667h; Title compound not separated from byproducts; | A 0.4 % Chromat. B 94.7 % Chromat. |
2,4-dinitrotoluene
A
2,4,6-Trinitrotoluene
B
1-bromo-2-methyl-3,5-dinitrobenzene
C
1-chloro-2-methyl-3,5-dinitrobenzene
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid; chlorine at 90℃; for 0.8h; Rate constant; Mechanism; Product distribution; further reaction times; oleum instead of sulphuric acid; | A 19.1 % Chromat. B 8.8 % Chromat. C 52.3 % Chromat. |
Conditions | Yield |
---|---|
With sodium methylate In methanol at 25℃; Equilibrium constant; Rate constant; |
Conditions | Yield |
---|---|
With sodium methylate In methanol at 25℃; Equilibrium constant; Rate constant; |
Conditions | Yield |
---|---|
With sodium methylate In methanol at 25℃; Equilibrium constant; Rate constant; |
Conditions | Yield |
---|---|
With sodium methylate In methanol at 25℃; Equilibrium constant; Rate constant; |
Conditions | Yield |
---|---|
With sodium methylate In methanol at 25℃; Equilibrium constant; Rate constant; |
Conditions | Yield |
---|---|
With Isopropylamine hydroperchlorate In dimethyl sulfoxide at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
With n-butylammonium perchlorate In dimethyl sulfoxide at 25℃; Equilibrium constant; |
2,4,6-Trinitrotoluene
Conditions | Yield |
---|---|
With sodium sulfite In water at 25℃; Equilibrium constant; variation with solvent composition; |
Conditions | Yield |
---|---|
With piperidine hydrochloride In dimethyl sulfoxide at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
With benzylamine hydrogenperchlorate In dimethyl sulfoxide at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
In acetonitrile at 25℃; Rate constant; different solvents; |
Conditions | Yield |
---|---|
In methanol; dimethyl sulfoxide at 25℃; Rate constant; Equilibrium constant; |
Conditions | Yield |
---|---|
unter azeotropem Abdestillieren des entstehenden Wassers; | |
in der Waerme bei groesserer Konzentration der Salpetersaeure; | |
unter azeotropem Abdestillieren des entstehenden Wassers; |
Conditions | Yield |
---|---|
in der Waerme; |
4-methylisopropylbenzene
sulfuric acid
nitric acid
A
2,4,6-Trinitrotoluene
B
3,5-dinitro-p-toluic acid
Conditions | Yield |
---|---|
at 60 - 70℃; |
Conditions | Yield |
---|---|
With piperidine In benzene for 12h; Knoevenagel Condensation; Dean-Stark; Reflux; | 95.1% |
2,4,6-Trinitrotoluene
1-nitromethyl-2,4,6-trinitrobenzene
Conditions | Yield |
---|---|
With potassium hydroxide; fluorotrinitromethane In tetrahydrofuran; methanol; water for 0.0333333h; Nitration; | 95% |
2,4,6-Trinitrotoluene
Conditions | Yield |
---|---|
Stage #1: 2,4,6-Trinitrotoluene With hydrogen; pyrographite In methanol at 120℃; under 45004.5 Torr; for 5h; Large scale; Stage #2: With hydrogenchloride In water for 1h; Reagent/catalyst; Solvent; Pressure; Large scale; | 95% |
2,4,6-Trinitrotoluene
2,4,6-trinitrobenzaldehyde
2,2’,4,4’,6,6’-hexanitrostilbene
Conditions | Yield |
---|---|
With piperidine In toluene Reflux; | 94.2% |
2,4,6-Trinitrotoluene
Conditions | Yield |
---|---|
Stage #1: 2,4,6-Trinitrotoluene With hydrogen In toluene at 120℃; under 30003 Torr; for 10h; Autoclave; Stage #2: With hydrogenchloride In water for 0.5h; Solvent; Pressure; Temperature; | 93.1% |
Conditions | Yield |
---|---|
With piperidine In benzene for 14h; Knoevenagel Condensation; Dean-Stark; Reflux; | 90.3% |
Conditions | Yield |
---|---|
With piperidine In benzene for 6h; Knoevenagel Condensation; Dean-Stark; Reflux; | 90.2% |
3-methylisoquinoline
2,4,6-Trinitrotoluene
benzoyl chloride
[3-Methyl-1-(2,4,6-trinitro-benzyl)-1H-isoquinolin-2-yl]-phenyl-methanone
Conditions | Yield |
---|---|
In chloroform at 60 - 70℃; for 1h; | 90% |
Conditions | Yield |
---|---|
With hydrogenchloride; palladium on activated charcoal; hydrogen In methanol at 20℃; under 18751.9 Torr; for 2h; Solvent; Pressure; Time; | 90% |
With iron(III) chloride; pyrographite; hydrazine hydrate In methanol for 7h; Heating; | 67.8% |
2,4,6-Trinitrotoluene
3-formyl-4,6-dinitro-1-phenyl-1H-indazole
Conditions | Yield |
---|---|
With potassium carbonate In ethanol at 20℃; for 24h; | 90% |
Conditions | Yield |
---|---|
90% | |
In toluene at 20℃; for 24h; | 70% |
Conditions | Yield |
---|---|
With piperidine In benzene for 11h; Knoevenagel Condensation; Dean-Stark; Reflux; | 89.5% |
Conditions | Yield |
---|---|
With sodium chlorate; nitric acid | 88% |
With sodium dichromate; sulfuric acid at 45 - 55℃; for 2h; Oxidation; | 14% |
With sodium chlorate; nitric acid Reinigung ueber das Natrium-Salz; |
2,4,6-Trinitrotoluene
benzaldehyde
1,3,5-trinitro-2-[(E)-2-phenylvinyl]benzene
Conditions | Yield |
---|---|
With piperidine; silica gel In neat (no solvent) at 120℃; for 0.333333h; Microwave irradiation; | 88% |
With piperidine In benzene for 6h; Condensation; Heating; | 81% |
With HTc-4-Cal In toluene for 15h; Reagent/catalyst; Time; Reflux; Dean-Stark; | 70% |
With piperidine | |
With piperidine; ethanol at 40℃; |
2,4,6-Trinitrotoluene
Methyl thioglycolate
A
2,4-dinitro-6-[(methoxycarbonyl)methylthio]toluene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 20℃; for 24h; | A 88% B n/a |
2,4,6-Trinitrotoluene
4-chlorobenzaldehyde
2-[(E)-2-(4-Chloro-phenyl)-vinyl]-1,3,5-trinitro-benzene
Conditions | Yield |
---|---|
With piperidine In benzene for 5.5h; Knoevenagel Condensation; Dean-Stark; Reflux; | 87.6% |
Conditions | Yield |
---|---|
With piperidine In benzene for 6h; Knoevenagel Condensation; Dean-Stark; Reflux; | 87% |
Ethyl 2-mercaptopropionate
2,4,6-Trinitrotoluene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 20℃; for 24h; | A 86% B n/a |
2,4,6-Trinitrotoluene
2,4,6-trinitro(α,αα-D3)toluene
Conditions | Yield |
---|---|
With tributyl-amine; water-d2 In N,N-dimethyl-formamide for 5h; | 85% |
With [(2)H6]acetone; deuteromethanol; water-d2; triethylamine for 1.5h; Ambient temperature; | 63% |
2,4,6-Trinitrotoluene
ethane-1,2-dithiol
1,2-bis((2-methyl-3,5-dinitrophenyl)thio)ethane
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h; | 85% |
2,4,6-Trinitrotoluene
ethyl 2-sulfanylacetate
(2-methyl-3,5-dinitro-phenylsulfanyl)-acetic acid ethyl ester
Conditions | Yield |
---|---|
With alkaline resin In acetone at 50℃; for 20h; Large scale; | 85% |
2,4,6-Trinitrotoluene
4-methoxy-benzaldehyde
2-[(E)-2-(4-methoxyphenyl)vinyl]-1,3,5-trinitrobenzene
Conditions | Yield |
---|---|
With HTc-4-Cal In toluene for 24h; Knoevenagel Condensation; Reflux; Dean-Stark; | 83% |
With piperidine In benzene for 6h; Condensation; Heating; | 60% |
With piperidine |
Conditions | Yield |
---|---|
With piperidine; silica gel In neat (no solvent) at 120℃; for 0.333333h; Microwave irradiation; | 83% |
With HTc-4-Cal In toluene for 24h; Knoevenagel Condensation; Reflux; Dean-Stark; | 71% |
1-thiopropane
2,4,6-Trinitrotoluene
(2-methyl-3,5-dinitrophenyl)(propyl)sulfane
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h; | 83% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; | 83% |
Conditions | Yield |
---|---|
With piperidine; silica gel In neat (no solvent) at 120℃; for 0.333333h; Microwave irradiation; | 82% |
With piperazine at 80 - 90℃; |
2,4,6-Trinitrotoluene
4-chlorobenzaldehyde
trans-4′-chloro-2,4,6-trinitrostilbene
Conditions | Yield |
---|---|
With piperidine; silica gel In neat (no solvent) at 120℃; for 0.333333h; Microwave irradiation; | 82% |
With HTc-4-Cal In toluene for 24h; Knoevenagel Condensation; Reflux; Dean-Stark; | 70% |
With piperidine at 120℃; |
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