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roduct Name: 3-Nitrotoluene Synonyms: m-mononitrotoluene;m-nitro-toluen;MNT;nsc9578;Toluene, m-nitro-;toluene,3-nitro-;3-NITROTOLUENE;3-METHYLNITROBENZENE CAS: 99-08-1 MF
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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inquiry3-Nitrotoluene CAS. NO.99-08-1 Application:3-Nitrotoluene CAS. NO.99-08-1
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Conditions | Yield |
---|---|
With sodium tetrahydroborate; sodium hydroxide In water at 60℃; for 1.5h; pH=12; Reagent/catalyst; Green chemistry; | 99% |
With diethylzinc; tetrakis(triphenylphosphine) palladium(0) In hexane; N,N-dimethyl-formamide at 25℃; for 1h; | 63% |
With lithium aluminium tetrahydride In diethyl ether at 0℃; for 1.5h; | 72 % Turnov. |
m-tolylboronic acid
1-methyl-3-nitrobenzene
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; bismuth (III) nitrate pentahydrate In toluene at 80℃; for 12h; Inert atmosphere; | 96% |
With N-Bromosuccinimide; [bis(trifluoroacetoxy)iodo]benzene; sodium nitrite In acetonitrile at 20℃; for 3h; Solvent; regioselective reaction; | 93% |
With pyridine; copper(I) oxide; sodium nitrite In acetonitrile at 20℃; | 78% |
Conditions | Yield |
---|---|
With 1,9-diperoxynonanedioic acid In acetonitrile at 50℃; for 0.5h; | 95% |
With dihydrogen peroxide; acetonitrile In aq. buffer at 20℃; for 1h; pH=11; Green chemistry; | 88% |
With sodium perborate tetrahydrate; cetyltrimethylammonim bromide In water at 60℃; for 12h; silica gel; Micellar solution; Green chemistry; regioselective reaction; | 53% |
With sulfuric acid Diazotization.Behandlung der neutralisierten Diazoniumsalz-Loesung mit NaNO2 und Kupfer(I)-kupfer(II)-sulfit; | |
With sulfuric acid Diazotization.Behandlung der neutralisierten Diazoniumsalz-Loesung mit NaNO2, CuSO4 und Cu2O; |
Conditions | Yield |
---|---|
palladium diacetate In tetrahydrofuran at 40℃; for 0.25h; | 90% |
2-methyl-6-nitrobenzoic acid
1-methyl-3-nitrobenzene
Conditions | Yield |
---|---|
With silver carbonate In dimethyl sulfoxide at 120℃; for 16h; | 86% |
With silver carbonate In dimethyl sulfoxide at 120℃; | |
Multi-step reaction with 3 steps 1.1: sodium hydroxide / tetrahydrofuran; water / 0.17 h / Darkness 1.2: 0.08 h / Darkness 2.1: acetonitrile / 0.08 h / Darkness 3.1: water / d7-N,N-dimethylformamide / 2 h / 100 °C / Inert atmosphere; Glovebox; Sealed tube; Darkness View Scheme |
Conditions | Yield |
---|---|
With nitric acid; sodium dodecyl-sulfate In acetonitrile at 24.84℃; for 3h; Micellar solution; regioselective reaction; | 85% |
4-methyl-2-nitrobenzoic acid
1-methyl-3-nitrobenzene
Conditions | Yield |
---|---|
With copper(l) iodide; triethylamine In dimethyl sulfoxide at 120℃; under 760.051 Torr; for 20h; Inert atmosphere; Schlenk technique; | 85% |
With 1-methyl-pyrrolidin-2-one; quinoline; copper(I) oxide; 1,10-Phenanthroline at 100 - 175℃; for 0.5h; Inert atmosphere; Microwave irradiation; | 50% |
Multi-step reaction with 3 steps 1: tetrahydrofuran / 2 h / 20 °C / Darkness 2: tetrahydrofuran / Darkness 3: water / d7-N,N-dimethylformamide / 0.83 h / 100 °C / Inert atmosphere; Glovebox; Sealed tube; Darkness View Scheme |
Conditions | Yield |
---|---|
With copper; tetrabutylammonium nitrite; N,N`-dimethylethylenediamine In N,N-dimethyl-formamide at 110℃; for 0.333333h; Inert atmosphere; Microwave irradiation; | 84% |
With copper bronze; tetrabutylammonium nitrate; N,N`-dimethylethylenediamine In N,N-dimethyl-formamide at 100℃; | 69% |
With potassium nitrite; copper(II) bis(trifluoromethanesulfonate) In dimethyl sulfoxide at 130℃; for 48h; Inert atmosphere; Sealed tube; regioselective reaction; | 67% |
Conditions | Yield |
---|---|
With dichloro bis(1,4-diazabicyclo[2.2.2]octane)(BH4)Zr(IV); toluene-4-sulfonic acid In sulfolane; N,N-dimethyl-formamide at 110℃; for 7.2h; | 83% |
Conditions | Yield |
---|---|
With palladium diacetate In water at 60 - 70℃; for 4h; | 80% |
palladium diacetate In water at 60℃; for 4h; | 80 % Chromat. |
toluene
A
1-methyl-3-nitrobenzene
B
1-methyl-4-nitrobenzene
C
1-methyl-2-nitrobenzene
Conditions | Yield |
---|---|
With copper(II) nitrate on K10 montmorillonite; acetic anhydride In tetrachloromethane for 120h; Ambient temperature; | A 1% B 79% C 20% |
With nitric acid In trifluoroacetic acid at 25℃; Rate constant; | A 0.7% B 66.7% C 32.6% |
With ortho-methylphenyl iodide; potassium nitrate In trifluoroacetic acid for 0.5h; Product distribution; nitration of aromatic compounds in the presence of aryl iodides; other temperatures, other reagents; | A n/a B 64% C 33% |
Conditions | Yield |
---|---|
With palladium diacetate In N,N-dimethyl-formamide at 60 - 70℃; for 2.5h; | 77% |
palladium diacetate In N,N-dimethyl-formamide at 60℃; for 2h; | 77 % Chromat. |
Conditions | Yield |
---|---|
With palladium diacetate In N,N-dimethyl-formamide at 60 - 70℃; for 2.5h; | 77% |
palladium diacetate In N,N-dimethyl-formamide at 60℃; for 2.5h; | 77 % Chromat. |
Conditions | Yield |
---|---|
With [Au(1,3-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazol-2-ylidene)(O2CAd)] In toluene at 140℃; for 20h; | 71% |
diisopropyl hydrogenphosphonate
1-bromomethyl-3-nitrobenzene
A
1-methyl-3-nitrobenzene
Conditions | Yield |
---|---|
With sodium hydride In isopropyl alcohol for 3h; Ambient temperature; | A 21% B 69% |
toluene
A
1-methyl-3-nitrobenzene
B
1-methyl-4-nitrobenzene
C
1-methyl-2-nitrobenzene
Conditions | Yield |
---|---|
Product distribution; Ambient temperature; | A 3% B 32% C 65% |
tetramethylstannane
m-nitrobenzenediazonium hexafluorophosphate
1-methyl-3-nitrobenzene
Conditions | Yield |
---|---|
palladium diacetate In acetonitrile for 2h; Ambient temperature; | 62% |
2-(3-nitrophenyl)acetaldehyde
A
1-methyl-3-nitrobenzene
B
3-nitro-benzaldehyde
C
3,3'-dinitrobibenzyl
Conditions | Yield |
---|---|
In water; acetonitrile for 48h; Product distribution; Irradiation; | A 60% B 40% C n/a |
m-toluidine hydrochloride
A
1-methyl-3-nitrobenzene
B
1-chloro-2-methyl-4-nitrobenzene
Conditions | Yield |
---|---|
With 3,3-dimethyldioxirane In acetone at 20℃; | A 45% B 55% |
2-iodo-5-nitrotoluene
A
1-methyl-3-nitrobenzene
B
2,2'-dimethyl-4,4'-dinitro-biphenyl
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 100℃; for 12h; Catalytic behavior; Ullmann Condensation; Inert atmosphere; Green chemistry; | A 10% B 55% |
1-bromomethyl-3-nitrobenzene
A
1-methyl-3-nitrobenzene
B
3,3'-dinitrobibenzyl
Conditions | Yield |
---|---|
With diisopropyl phosphite; sodium hydride In tetrahydrofuran for 3h; Ambient temperature; | A 5% B 28% C 52% |
toluene
A
1-methyl-3-nitrobenzene
B
1-methyl-4-nitrobenzene
C
1-methyl-2-nitrobenzene
D
2,4-dinitrotoluene
Conditions | Yield |
---|---|
With trinitratooxovanadium(V) In dichloromethane for 0.05h; Ambient temperature; Further byproducts given; | A 3% B 47% C 50% D n/a |
With trinitratooxovanadium(V) In dichloromethane for 0.1h; Ambient temperature; Further byproducts given; | A 2% B 41% C 35% D 19% |
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; ammonium iodide; water In dimethyl sulfoxide at 90℃; for 4h; Sealed tube; | 38% |
toluene
A
1-methyl-3-nitrobenzene
B
1-methyl-4-nitrobenzene
C
1-methyl-2-nitrobenzene
D
benzaldehyde
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate In water; trifluoroacetic acid for 72h; Ambient temperature; Yield given; | A n/a B n/a C n/a D 24.5% |
With nitric acid at 90 - 100℃; for 4h; Product distribution; Further Variations:; Temperatures; Reagents; | |
With nitrogen dioxide at 70℃; for 6h; Reagent/catalyst; Autoclave; Green chemistry; |
dibenzylphosphine oxide
1-bromomethyl-3-nitrobenzene
A
1-methyl-3-nitrobenzene
B
3,3'-dinitrobibenzyl
Conditions | Yield |
---|---|
With sodium hydride 1.) THF, 2.) THF, RT, 3 h; Yield given. Multistep reaction; | A 2% B 21% C n/a |
Conditions | Yield |
---|---|
at 170℃; im geschlossenen Rohr; |
methyl radical
nitrobenzene
A
1-methyl-3-nitrobenzene
B
1-methyl-4-nitrobenzene
C
1-methyl-2-nitrobenzene
Conditions | Yield |
---|---|
at 143℃; |
Conditions | Yield |
---|---|
With hydrogenchloride Diazotization.Behandlung der Diazoniumsalz-Loesung mit wss.-alkal. Natriumstannit-Loesung bei -10grad; | |
Diazotization.Erwaermen des Diazoniumsulfats mit Alkohol; | |
With formamide; triethylamine; trifluoroacetic acid; sodium nitrite 1.) formamide/water, r.t.; 2.) water, r.t.; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
durch Entamidierung; | |
With hydrogenchloride Diazotization.Behandlung der Diazoniumsalz-Loesung mit H3PO2; | |
Diazotization.Kochen des Diazoniumsulfats mit absol. Alkohol; |
Conditions | Yield |
---|---|
With laccase from Coriolus versicolor MTCC-138; 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt In 1,4-dioxane for 1h; pH=4.5; Green chemistry; Enzymatic reaction; | 100% |
With laccase at 20℃; Reagent/catalyst; Green chemistry; Enzymatic reaction; | 100% |
With laccase of Pleurotus ostreatus MTCC-1801; 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt In 1,4-dioxane at 20℃; pH=4.5; Enzymatic reaction; | 98% |
Conditions | Yield |
---|---|
With [1-butyl-2,3-dimethylimidazolium][tppm] stabilized rhodium nanoarticles at 50℃; under 22502.3 Torr; for 5h; Ionic liquid; Autoclave; chemoselective reaction; | 100% |
With cadmium sulphide; ammonium formate In water at 20℃; for 14h; Inert atmosphere; Irradiation; Sealed tube; | 100% |
With water; oxalic acid; titanium(IV) oxide for 3h; Wavelength; Irradiation; Inert atmosphere; Sealed tube; Green chemistry; chemoselective reaction; | 100% |
propyl cyanide
1-methyl-3-nitrobenzene
A
N-butyl-m-toluidine
B
N-butyl-N-(3-methyl-n-propyl)-m-toluidine
Conditions | Yield |
---|---|
Stage #1: 1-methyl-3-nitrobenzene With ammonium formate; palladium on activated charcoal In methanol; water at 20℃; Stage #2: propyl cyanide In methanol; water | A 100% B n/a |
Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In water; isopropyl alcohol at 20℃; for 1h; | 100% |
1-methyl-3-nitrobenzene
2,5-hexanedione
N-(3′-methylphenyl)-2,5-dimethylpyrrole
Conditions | Yield |
---|---|
With formic acid for 12h; Autoclave; Inert atmosphere; Green chemistry; | 100% |
With indium; acetic acid In toluene at 80℃; for 3h; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
Stage #1: 1-methyl-3-nitrobenzene With hydrogen In ethanol at 25℃; under 11172.7 Torr; Flow reactor; Stage #2: With hydrogenchloride In ethanol Flow reactor; chemoselective reaction; | 99% |
With hydrogenchloride; tin(ll) chloride In ethanol; water at 30℃; Rate constant; Mechanism; various concentration of HCl; | |
Stage #1: 1-methyl-3-nitrobenzene With phosgene; sodium tetrahydroborate; copper(II) sulfate In methanol at 20℃; Stage #2: With hydrogenchloride In methanol; diethyl ether | 550 mg |
Conditions | Yield |
---|---|
With indium; acetic acid In methanol at 20℃; for 1h; | 99% |
Stage #1: 1-methyl-3-nitrobenzene With sodium tetrahydroborate In water at 60 - 70℃; Green chemistry; Stage #2: acetic anhydride In water at 60 - 70℃; Green chemistry; | 94% |
Stage #1: 1-methyl-3-nitrobenzene In water for 0.0833333h; Stage #2: With sodium tetrahydroborate In water at 65℃; for 0.05h; Stage #3: acetic anhydride In water at 65℃; for 0.0333333h; Catalytic behavior; | 93% |
tungsten hexacarbonyl
1-methyl-3-nitrobenzene
carbonic acid dimethyl ester
3-Methylacetanilide
Conditions | Yield |
---|---|
With di(rhodium)tetracarbonyl dichloride; 1,3-bis-(diphenylphosphino)propane; sodium phosphate; sodium iodide In water at 120℃; for 24h; Inert atmosphere; Sealed tube; | 99% |
Conditions | Yield |
---|---|
With 1,3-bis(N',N'-dimethyl-4-aminopyridinium)propane diiodide; sodium hydride In N,N-dimethyl-formamide; paraffin oil at 20℃; for 0.25h; Inert atmosphere; | 98% |
With potassium hydroxide In water; isopropyl alcohol at 35℃; under 760.051 Torr; for 8h; Inert atmosphere; | 95% |
With Piperonyl butoxide; ammonium formate In methanol for 1.25h; Heating; | 94% |
1-methyl-3-nitrobenzene
5-(3-nitrophenyl)-1H-tetrazole
Conditions | Yield |
---|---|
With sodium azide; hydroxylamine hydrochloride In water at 20℃; for 4.16667h; | 97% |
phenyl benzyl ketone
1-methyl-3-nitrobenzene
2-(3-methylphenyl)-1,2-diphenylethanone
Conditions | Yield |
---|---|
With potassium phosphate; bis(acetylacetonato)palladium(II); dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine In cyclohexane at 130℃; for 24h; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
With gold nano particles supported on rutile TiO2 In toluene at 70℃; under 750.075 Torr; for 3h; Inert atmosphere; chemoselective reaction; | 96% |
With cobalt nanoparticles anchoring on nitrogen doped carbon, pyrolysis at 700 °C In acetonitrile at 110℃; under 750.075 Torr; for 5h; Inert atmosphere; chemoselective reaction; | 96.2% |
With palladium(II) trifluoroacetate; triphenylphosphine In water at 80℃; for 0.333333h; Sealed tube; Green chemistry; | 92% |
With [PdCl4]2-ion-exchanged imidazolium IL containing triethylene glycol-tagged onto silica-coated iron oxide nanoparticles In water at 90℃; for 24h; Inert atmosphere; Green chemistry; | |
With palladium particles distributed over the surface of fibrous silica nanospheres modified via aminopropyltriethoxysilane In toluene at 70℃; for 3h; | 98 %Chromat. |
Conditions | Yield |
---|---|
With methyldiazene In acetonitrile at 28℃; for 1.33333h; Irradiation; Sealed tube; Inert atmosphere; | 95% |
With sodium tetrahydroborate; palladium diacetate In ethanol; dichloromethane; water at 20℃; for 0.0833333h; | 88% |
With rhodium contaminated with carbon; hydrazine hydrate In tetrahydrofuran at 0 - 20℃; for 3h; | 85% |
1-methyl-3-nitrobenzene
A
1-amino-3-methylbenzene
B
3,3'-dimethylhydrazobenzene
Conditions | Yield |
---|---|
With potassium hydroxide; aluminium In methanol at 20℃; for 0.25h; Reduction; Reductive coupling; | A 3% B 95% |
Conditions | Yield |
---|---|
With hydrogen In toluene at 140℃; under 30003 Torr; for 3h; chemoselective reaction; | 95% |
1-methyl-3-nitrobenzene
3,3'-dimethylazoxybenzene
Conditions | Yield |
---|---|
With oxygen; ammonium chloride; zinc In [bmim][BF4]; water at 20℃; for 16h; | 94% |
With potassium hydroxide In methanol; toluene for 24h; Heating; | 90% |
Stage #1: 1-methyl-3-nitrobenzene With sodium tetrahydroborate; palladium diacetate In ethanol; dichloromethane; water at 20℃; Stage #2: With oxygen In ethanol; dichloromethane; water | 90% |
1-methyl-3-nitrobenzene
ammonium formate
N-formyl-m-toluidine
Conditions | Yield |
---|---|
With cobalt nanoparticles coated by N,P-codoped carbon shell pyrolyzed at 800°C In tetrahydrofuran at 120℃; for 12h; Schlenk technique; Inert atmosphere; | 94% |
With zinc for 0.05h; microwave irradiation; | 80% |
1-methyl-3-nitrobenzene
1-phenylpentane-1,4-dione
2-methyl-5-phenyl-1-m-tolyl-1H-pyrrole
Conditions | Yield |
---|---|
With indium; acetic acid In toluene for 0.5h; Inert atmosphere; Reflux; | 94% |
Conditions | Yield |
---|---|
With ruthenium trichloride; sodium hypochlorite; tetrabutylammomium bromide In 1,2-dichloro-ethane at 25℃; for 2h; | 93% |
With chromium(VI) oxide; periodic acid In acetonitrile at 20℃; for 1h; | 93% |
With oxygen; acetic acid; 1N,3N,5N-trihydroxy-1,3,5-triazin-2,4,6[1H,3H,5H]-trione; cobalt(II) acetate; manganese(II) acetate at 100℃; under 760 Torr; for 14h; | 88% |
1-methyl-3-nitrobenzene
trans-3,3'-dimethylazobenzene
Conditions | Yield |
---|---|
With ammonium acetate; lead In methanol at 20℃; | 93% |
With isopropyl alcohol; sodium hydroxide at 30℃; for 2h; Catalytic behavior; Inert atmosphere; UV-irradiation; | 88% |
With ethanolamine; potassium hydroxide at 55℃; for 1h; Sonication; Microwave irradiation; | 88% |
Conditions | Yield |
---|---|
With formic acid; Au/TiO2-R In water at 80℃; under 760.051 Torr; for 4h; Inert atmosphere; Green chemistry; chemoselective reaction; | 93% |
With hydrogen In ethanol at 120℃; under 15001.5 Torr; for 8.5h; Autoclave; | 87% |
Stage #1: 1-methyl-3-nitrobenzene With triethylsilane; palladium In methanol at 20℃; under 760.051 Torr; for 2h; Stage #2: benzaldehyde In methanol | 70% |
Conditions | Yield |
---|---|
With potassium tert-butylate at 130℃; for 24h; Sealed tube; | 93% |
With [(N,N′-bis(diisopropylphosphino)-2,6-diaminopyridine)Mn(CO)3][Br]; potassium hydroxide at 110℃; for 16h; Molecular sieve; Sealed tube; | 80% |
With [Ru(2-(6-methoxypyridin-2-yl)-1,10-phenanthroline)(MeCN)2Cl]Cl; sodium methylate at 110℃; for 12h; Green chemistry; | 87 %Chromat. |
With platinum on carbon; potassium tert-butylate; hydrogen at 150℃; under 1500.15 Torr; for 24h; Autoclave; | 93 %Chromat. |
1-methyl-3-nitrobenzene
2,2,2-trifluoro-N-(2-iodophenyl)acetimidoyl chloride
molybdenum hexacarbonyl
Conditions | Yield |
---|---|
With 1,3-bis-(diphenylphosphino)propane; sodium carbonate; palladium dichloride In 1,4-dioxane at 120℃; for 24h; Inert atmosphere; Sealed tube; | 93% |
Conditions | Yield |
---|---|
With N-acetoxyphthalimide; cobalt(II) acetate; manganese(II) acetate In acetic acid at 130℃; under 7600 Torr; for 14h; | A 5% B 92% |
With Coprinus sp. peroxidase; tartaric acid buffer; dihydrogen peroxide In water; acetone at 20℃; pH=5; |
Conditions | Yield |
---|---|
With samarium diiodide In tetrahydrofuran at 20℃; for 0.5h; | 92% |
Conditions | Yield |
---|---|
With palladium diacetate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In 1-methyl-pyrrolidin-2-one at 150℃; for 24h; Inert atmosphere; Sealed vessel; | 92% |
With N/O-doped porous carbon (on base of polypyrrole) supported nanopalladium at 80℃; Inert atmosphere; | 70% |
1-methyl-3-nitrobenzene
A
3,3'-dimethylazobenzene
B
3,3'-dimethylazoxybenzene
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate; diphenyl ditelluride In ethanol for 20h; Heating; | A 90% B 10% |
With sodium tetrahydroborate; water In ethanol at 30℃; for 3h; chemoselective reaction; | A n/a B 78% |
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