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1-Chloro-2,4-dinitrobenzene Application:817802
Cas:97-00-7
Min.Order:1 Gram
FOB Price: $500.0
Type:Trading Company
inquiryConditions | Yield |
---|---|
With sulfuric acid; nitric acid at 25℃; Product distribution; variation of oleum concentration; | 100% |
Stage #1: 4-chlorobenzonitrile With nitric acid at 20℃; Stage #2: With sulfuric acid for 0.5h; | 96% |
With trifluoromethylsulfonic anhydride; ethylammonium nitrate at 0 - 40℃; for 9h; Inert atmosphere; regioselective reaction; | 78% |
chlorobenzene
A
1-chloro-2,6-dinitrobenzene
B
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With Perfluorooctanesulfonic acid; nitric acid; ytterbium(III) perfluorooctanesulfonate In hexane at 60℃; for 18h; | A 3% B 97% |
With Nitrogen dioxide In dichloromethane at -10℃; Product distribution; Further Variations:; Reagents; Kyodai nitration; |
Conditions | Yield |
---|---|
With tungsten trioxide; disodium hydrogenphosphate; NaMoO4; nitric acid; sodium carbonate at 55 - 70℃; for 24h; Temperature; | 94.9% |
With sulfuric acid; nitric acid | |
With sulfuric acid; potassium nitrate man giesst auf Eis und krystallisiert aus Alkohol um; |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; N-benzyl-N,N,N-triethylammonium chloride; sodium nitrite In tetrachloromethane 1.) 0 deg C, 1.5 h, 2.) r.t., 14 h; | 92% |
With nitrosylsulfuric acid; phosphoric acid; sulfuric acid Diazotization.Behandlung der Diazoniumsalz-Loesung mit CuCl in konz. wss. HCl; |
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride In acetonitrile at 20℃; for 0.75h; Substitution; | 90% |
Multi-step reaction with 2 steps 1: 94 percent / aq. NaOH / 0.5 h / 0 - 5 °C 2: 77 percent / aq. HCl; HBF4; Cu / acetonitrile / 2 h / 60 °C View Scheme |
(2,4-dinitro-phenyl)-hydrazine
A
meta-dinitrobenzene
B
2,4-dinitrobromobenzene
C
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With ammonium cerium (IV) nitrate; 1,2-dibromo-1,1,2,2-tetrachloroethane In methanol at 20℃; for 0.0833333h; | A 80% B 10% C 1% |
Conditions | Yield |
---|---|
With phosphorus pentoxide; N,N-dimethyl-formamide; zinc(II) chloride at 60 - 70℃; for 1h; | 78% |
With N,N-diethylaniline; trichlorophosphate | |
With phosphorus pentachloride | |
With trichlorophosphate In N,N-dimethyl-formamide for 2h; Ambient temperature; |
Conditions | Yield |
---|---|
With hydrogenchloride; tetrafluoroboric acid; copper In acetonitrile at 60℃; for 2h; | A 5% B 77% |
4-Chlorophenylboronic acid
A
4-chlorobenzonitrile
B
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With ammonium nitrate; trifluoroacetic anhydride In acetonitrile at -35℃; for 6h; Nitration; Ipso-nitration; | A 32% B 46% |
1-chloro-3-hydrazino-4,6-dinitrobenzene
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With ethanol; copper(II) sulfate |
A
(E)-styrylaldehyde oxime
B
1-chloro-2,4-dinitro-benzene
1-(2,4-dinitrophenyl)-pyridinium chloride
A
pyridine
B
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
beim Schmelzen; |
2-Chloronitrobenzene
A
1-chloro-2,6-dinitrobenzene
B
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid | |
With sulfuric acid; nitric acid | |
With H-Faujasite 720; dinitrogen pentoxide In dichloromethane at 0℃; for 2h; Kinetics; Further Variations:; Reagents; Nitration; |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid | |
With sulfuric acid; nitric acid | |
With boron trifluoride; nitric acid |
Conditions | Yield |
---|---|
With N,N-diethylaniline |
Conditions | Yield |
---|---|
With quinoline |
Conditions | Yield |
---|---|
With chlorine fluorosulfate at 25℃; |
meta-dinitrobenzene
A
1,3,5-trinitrobenzene
B
1-chloro-3,5-dinitrobenzene
C
2,5-dichloro-1,3-dinitrobenzene
D
1,2-dichloro-3,5-dinitrobenzene
E
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With hydrogenchloride; sulfuric acid; nitric acid at 130℃; for 0.166667h; Rate constant; Product distribution; | |
With hydrogenchloride; sulfuric acid; nitric acid at 130℃; for 0.166667h; Rate constant; Product distribution; |
2-chloro-5-nitrobenzoic acid
A
2-chloro-3,5-dinitrobenzoic acid
B
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With nitric acid; dinitrogen pentoxide at 25℃; Product distribution; |
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With hydroxide In water; dimethyl sulfoxide at 25℃; Equilibrium constant; var. concentration of solvents; |
4-chlorobenzonitrile
A
3,4-dichloronitrobenzene
B
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid; chlorine at 25℃; Product distribution; HCl instead of Cl2; | A 2.4 % Chromat. B 97.8 % Chromat. |
2-Chloronitrobenzene
A
1,2-Dichloro-3-nitrobenzene
B
1-chloro-2,6-dinitrobenzene
C
1-chloro-2,4-dinitro-benzene
D
2,5-dichloronitrobenzene
Conditions | Yield |
---|---|
With hydrogenchloride; sulfuric acid; nitric acid at 25℃; Product distribution; | A 0.2 % Chromat. B 6.7 % Chromat. C 94.8 % Chromat. D 0.3 % Chromat. |
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
With sodium sulfite In water; dimethyl sulfoxide at 25℃; Equilibrium constant; investigation effect of solvent ratio; measured by spectrophotometer; |
Conditions | Yield |
---|---|
In cyclohexane at 21℃; Equilibrium constant; |
4-chloro-3-nitrobenzoate
A
1-chloro-2,4-dinitro-benzene
B
4-chloro-3,5-dinitrobenzoic acid
Conditions | Yield |
---|---|
With nitric acid; dinitrogen pentoxide at 25℃; Product distribution; addition of nitronium trifluoromethanesulphonate; |
methanol
1-(2,4-dinitrophenyl)-pyridinium chloride
A
pyridine
B
2,4-dinitroanisole
C
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
for 39h; Product distribution; Heating; |
A
3-methyl-4-(dimethylphenylsilyl)pyridine
B
1-chloro-2,4-dinitro-benzene
C
7-nitro-4-methyl-3-dimethylphenylsilylpyrido<1,2-a>benzimidazole
Conditions | Yield |
---|---|
With phenylhydrazine In acetic acid for 2h; Heating; Yield given. Yields of byproduct given; |
sulfuric acid
nitric acid
2-Chloronitrobenzene
1-chloro-2,4-dinitro-benzene
pyridine
1-chloro-2,4-dinitro-benzene
1-(2,4-dinitrophenyl)-pyridinium chloride
Conditions | Yield |
---|---|
In acetone Reflux; | 100% |
In acetone Reflux; | 97% |
at 95℃; for 1h; | 91% |
3-phenylpyridine
1-chloro-2,4-dinitro-benzene
N-(2',4'-dinitrophenyl)-3-phenylpyridinium chloride
Conditions | Yield |
---|---|
In acetone Reflux; | 100% |
In acetone for 48h; Heating; | 90% |
In acetone for 48h; Reflux; | 90% |
3-benzylpyridine
1-chloro-2,4-dinitro-benzene
N-(2,4-dinitrophenyl)-3-benzylpyridinium chloride
Conditions | Yield |
---|---|
In acetone Heating / reflux; | 100% |
With benzene |
3-Methylpyridine
1-chloro-2,4-dinitro-benzene
1-(2,4-dinitrophenyl)-3-methylpyridinium chloride
Conditions | Yield |
---|---|
In acetone | 100% |
In acetone Reflux; | 95% |
In acetone for 8h; Heating; | 92% |
4-methoxy-aniline
1-chloro-2,4-dinitro-benzene
N-(4-methoxyphenyl)-2,4-dinitrobenzenamine
Conditions | Yield |
---|---|
With sodium carbonate In ethanol Heating; | 100% |
In benzene at 40℃; Rate constant; Mechanism; other solvent; | |
With tetrabutyl-ammonium chloride In benzene at 30℃; Rate constant; different substrate concentrations; |
Conditions | Yield |
---|---|
In ethanol; water at 60℃; for 6h; | 100% |
In acetonitrile at 25℃; for 2h; Solvent; | 85% |
With ethanol | |
With sodium carbonate In acetone for 5h; Substitution; Heating; | |
In acetonitrile at 25℃; Kinetics; Solvent; |
Conditions | Yield |
---|---|
In ethanol at 20℃; for 15h; | 100% |
In ethanol; water at 20℃; for 1h; | 100% |
In ethanol at 0 - 20℃; for 15h; | 95% |
Conditions | Yield |
---|---|
With water; sodium hydroxide at 100℃; for 1.5h; | 100% |
With potassium carbonate In ethanol | 97.5% |
Stage #1: 1-chloro-2,4-dinitro-benzene With sodium hydroxide In water; acetonitrile for 1h; Reflux; Stage #2: With hydrogenchloride In water; acetonitrile Kinetics; Thermodynamic data; Solvent; Temperature; | 97% |
Conditions | Yield |
---|---|
With tin(II) chloride dihdyrate In ethanol at 20℃; | 100% |
With [Zn(BH4)2(py)] In tetrahydrofuran for 7h; Heating; | 95% |
With sodium tetrahydroborate In tetrahydrofuran; water at 20℃; for 6h; Catalytic behavior; Reagent/catalyst; Green chemistry; | 94% |
Conditions | Yield |
---|---|
With pyrographite; hydrazine hydrate In ethanol for 1.16667h; Time; Reflux; | 100% |
With hydrazine hydrate In ethanol for 3.5h; Reflux; | 91% |
With ammonium hydroxide; hydrazine hydrate |
dmap
1-chloro-2,4-dinitro-benzene
4-Dimethylamino-1-(2,4-dinitro-phenyl)-pyridinium; chloride
Conditions | Yield |
---|---|
In diethyl ether Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 21℃; for 2h; | 100% |
diphenyl diselenide
1-chloro-2,4-dinitro-benzene
(2,4-dinitrophenyl)(phenyl)selane
Conditions | Yield |
---|---|
With borax; N-Acetylcysteine In methanol; water for 1h; Ambient temperature; | 100% |
With sodium hydroxide; cetyltrimethylammonim bromide; Aminoiminomethanesulfinic acid In tetrahydrofuran for 4h; Heating; | 87% |
With sodium hydroxide; Aminoiminomethanesulfinic acid; cetyltrimethylammonim bromide In tetrahydrofuran; water for 4h; Heating; | 87% |
Stage #1: diphenyl diselenide With sodium tetrahydroborate In ethanol Inert atmosphere; Stage #2: 1-chloro-2,4-dinitro-benzene In ethanol; dimethyl sulfoxide for 12h; Reflux; Inert atmosphere; |
1-chloro-2,4-dinitro-benzene
diphenyldisulfane
2,4-dinitro-1-phenylsulfanyl-benzene
Conditions | Yield |
---|---|
With borax; N-Acetylcysteine In methanol; water for 1h; Ambient temperature; | 100% |
With sodium hydroxide; Aminoiminomethanesulfinic acid; cetyltrimethylammonim bromide In tetrahydrofuran; water for 4h; Product distribution; Heating; | 95% |
With sodium hydroxide; cetyltrimethylammonim bromide; Aminoiminomethanesulfinic acid In tetrahydrofuran for 4h; Heating; | 95% |
With sodium hydroxide; Aminoiminomethanesulfinic acid; cetyltrimethylammonim bromide In tetrahydrofuran; water for 4h; Heating; | 95% |
With aluminium trichloride; zinc In water; N,N-dimethyl-formamide at 65℃; for 6h; | 95% |
1-chloro-2,4-dinitro-benzene
2,4-dichlorophenol
2,4-dichloro-1-(2,4-dinitrophenoxy)benzene
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 20℃; | 100% |
With sodium hydroxide; tetrabutylammomium bromide In dichloromethane; water at 30℃; for 5h; | 91% |
1-Methoxy-2-(dimethyl-alanoxy)-ethan
1-chloro-2,4-dinitro-benzene
2,4-dinitrotoluene
Conditions | Yield |
---|---|
Pd(dippp)2 In benzene at 90℃; for 4.5h; Methylation; | 100% |
Conditions | Yield |
---|---|
With air; tetrabutylammomium bromide; potassium carbonate; [Pd(Cl)κ2N,C,-CH2C6H2(4,6-Me)2CH=NC6H3(2,6-iPr)2]2 In water for 3h; Suzuki-Miyaura coupling reaction; Heating; | 100% |
With tetra-n-propylammonium bromide; sodium carbonate In water at 100℃; for 0.5h; Catalytic behavior; Suzuki-Miyaura Coupling; | 100% |
With potassium carbonate; palladium diacetate In methanol; water at 20℃; for 4h; Suzuki cross-coupling; | 99% |
4-methoxyphenylboronic acid
1-chloro-2,4-dinitro-benzene
2,4-dinitro-4'-methoxybiphenyl
Conditions | Yield |
---|---|
With tetra-n-propylammonium bromide; sodium carbonate In water at 100℃; for 0.5h; Catalytic behavior; Suzuki-Miyaura Coupling; | 100% |
With potassium carbonate; palladium dichloride In various solvent(s) at 20℃; for 0.5h; Suzuki-Miyaura cross-coupling; | 98% |
With palladium diacetate; caesium carbonate at 80℃; for 8h; Suzuki coupling; | 80% |
With C43H54N2S; tetrabutylammomium bromide; palladium diacetate; potassium carbonate In water; isopropyl alcohol at 130℃; for 24h; Suzuki-Miyaura coupling reaction; Aerobic condition; Sealed tube; | 70% |
N-(2-pyridin-3-yl-ethyl)-benzamide
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
In butan-1-ol at 100℃; for 3h; | 100% |
Conditions | Yield |
---|---|
In acetone Heating / reflux; | 100% |
5-mercapto-3-phenyl-Δ(4)-{1,3,4}thiadiazoline-2-thione, potassium salt
1-chloro-2,4-dinitro-benzene
5-(2,4-dinitrophenylthio)-3-phenyl-1,3,4-thiadiazole-2(3H)-thione
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 24h; | 100% |
Conditions | Yield |
---|---|
In methanol for 24h; Reflux; | 100% |
5-methoxy-2-methylbenzo[d]thiazole
1-chloro-2,4-dinitro-benzene
C13H11N3O5S
Conditions | Yield |
---|---|
Stage #1: 5-methoxy-2-methylbenzo[d]thiazole With sodium hydroxide In water; ethylene glycol Reflux; Stage #2: 1-chloro-2,4-dinitro-benzene With acetic acid In ethanol; water; ethylene glycol for 5h; | 100% |
ethylenediamine
1-chloro-2,4-dinitro-benzene
N1-(2,4-dinitrophenyl)ethane-1,2-diamine hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydrogencarbonate In ethanol; water for 2h; Reflux; | 100% |
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
Stage #1: 1,1,1-trichloro-2-methylpropan-2-yl hydroxy(methyl)carbamate With sodium hydride In tetrahydrofuran at 0℃; for 1h; Schlenk technique; Inert atmosphere; Stage #2: 1-chloro-2,4-dinitro-benzene In tetrahydrofuran at 0 - 20℃; Schlenk technique; Inert atmosphere; | 100% |
4-methylphenylboronic acid
1-chloro-2,4-dinitro-benzene
4'-methyl-2,4-dinitro-1,1'-biphenyl
Conditions | Yield |
---|---|
With tetra-n-propylammonium bromide; sodium carbonate In water at 100℃; for 0.5h; Catalytic behavior; Suzuki-Miyaura Coupling; | 100% |
1-chloro-2,4-dinitro-benzene
2,2-dimethoxyethylamine
Conditions | Yield |
---|---|
With triethylamine In dimethyl sulfoxide at 100℃; for 0.0833333h; | 100% |
(R)-2-aminononane
1-chloro-2,4-dinitro-benzene
Conditions | Yield |
---|---|
In ethanol at 140℃; for 0.166667h; Microwave irradiation; | 100% |
[(1R)-1-cyclohexylethyl]amine
1-chloro-2,4-dinitro-benzene
(R)-N-(1-cyclohexylethyl)-2,4-dinitroaniline
Conditions | Yield |
---|---|
In ethanol at 140℃; for 0.166667h; Microwave irradiation; | 100% |
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