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inquiry5-Chloro-2-nitrobenzoic acid Basic information Product Name: 5-Chloro-2-nitrobenzoic acid Synonyms: RARECHEM AL BO 1106;TIMTEC-BB SBB009922;5-chloro-2-nitro-benzoicaci;Benzoic acid, 5-ch
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inquiryProduct Name 5-Chloro-2-nitrobenzoic acid Synonyms 5-Chloro-2-nitrobenzoic acid;2-Nitro-5-chlorobenzoic acid CAS: 2516-95-2 MF: - MW: -
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inquiryProduct Name: 5-Chloro-2-nitrobenzoic acid CAS: 2516-95-2 MF: C7H4ClNO4 MW: 201.56 EINECS: 219-738-1 Mol File: 2516-95-2.mol 5-Chloro-2-nitrobenzoic acid Structure 5-Chloro-2-nitrobenzoic acid Chemical Properties Melting point
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inquiryProduct name: 5-Chloro-2-Nitrobenzoic Acid CAS No.:2516-95-2 Molecule Formula:C7H4ClNO4 Molecule Weight:201.56 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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inquiry5-chloro-2-nitrobenzyl alcohol
5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen In 1,2-dichloro-ethane at 25℃; for 48h; Schlenk technique; | 87% |
5-chloro-2-nitrobenzyl alcohol
A
5-chloro-2-nitrobenzaldehyde
B
5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen In 1,2-dichloro-ethane at 25℃; for 48h; Schlenk technique; | A 22% B 60% |
Conditions | Yield |
---|---|
With potassium permanganate |
Conditions | Yield |
---|---|
With potassium permanganate | |
With potassium permanganate; tetrabutylammomium bromide |
3-chlorobenzoate
A
5-chloro-2-nitrobenzoic acid
B
3-chloro-2-nitro-benzoic acid
Conditions | Yield |
---|---|
With nitric acid | |
With nitric acid das Gemisch wird in Wasser von 50grad gegossen; | |
beim Nitrieren; |
ethyl 2-(5-chloro-2-nitrophenyl)-2-cyanoacetate
5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
With potassium permanganate; potassium carbonate |
diethyl 2-(5-chloro-2-nitrophenyl)propanedioate
5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
With potassium permanganate; potassium carbonate |
nitric acid
3-chlorobenzoate
A
5-chloro-2-nitrobenzoic acid
B
3-chloro-2-nitro-benzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: acetic acid; sodium acetate / bei der elektrolytischen Reduktion 2: hydrochloric acid 3: Verkochen des Diazoniumsulfatsmit Alkohol.Diazotization 4: potassium permanganate View Scheme |
4-hydroxylamino-2-nitrotoluene
5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: hydrochloric acid 2: Verkochen des Diazoniumsulfatsmit Alkohol.Diazotization 3: potassium permanganate View Scheme |
5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Verkochen des Diazoniumsulfatsmit Alkohol.Diazotization 2: potassium permanganate View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (i) NaOEt, DMSO, (ii) /BRN= 1451655/ 2: KMnO4, aq. K2CO3 View Scheme | |
Multi-step reaction with 2 steps 1: (i) NaOEt, DMSO, (ii) /BRN= 1451655/ 2: KMnO4, aq. K2CO3 View Scheme |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at -5 - 0℃; for 1h; | |
With nitric acid; acetic anhydride at 20℃; |
5-chloro-2-nitrobenzoic acid
5-chloro-2-nitrobenzoyl chloride
Conditions | Yield |
---|---|
With thionyl chloride | 100% |
With thionyl chloride Heating / reflux; | 98% |
With thionyl chloride In dichloromethane for 4h; Reflux; | 66% |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol under 735.5 Torr; for 2h; Ambient temperature; | 100% |
With hydrogen; nickel In ethanol at 20℃; | 96% |
Reduction; | 85% |
5-chloro-2-nitrobenzoic acid
5-chloro-2-nitrobenzyl alcohol
Conditions | Yield |
---|---|
With dimethylsulfide borane complex In tetrahydrofuran at 80℃; for 3h; Inert atmosphere; | 100% |
With borane-THF In tetrahydrofuran at 50℃; for 96h; | 91% |
With dimethylsulfide borane complex In tetrahydrofuran at 80℃; for 3h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol under 735.5 Torr; for 80h; | 100% |
5-chloro-2-nitrobenzoic acid
dimethyl sulfate
methyl 5-chloro-2-nitrobenzoate
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 0.5h; Esterification; Heating; | 100% |
With sodium carbonate In acetone for 3h; Heating; | 78% |
With potassium carbonate In acetone Reflux; | |
With potassium carbonate In [(2)H6]acetone for 0.5h; Reflux; | 534 g |
morpholine
5-chloro-2-nitrobenzoic acid
2-nitro-5-(morpholin-4-yl)benzoic acid
Conditions | Yield |
---|---|
Stage #1: morpholine; 5-chloro-2-nitrobenzoic acid at 110℃; for 2h; Neat (no solvent); Stage #2: pH=Ca. 3; Acidic aq. solution; | 100% |
at 120℃; for 6h; |
5-chloro-2-nitrobenzoic acid
dimethyl amine
5-dimethylamino-2-nitrobenzoic acid
Conditions | Yield |
---|---|
In water at 60℃; for 23h; | 99% |
In water at 0 - 60℃; for 23h; | 99% |
In water at 70℃; for 25h; Autoclave; | 99% |
In water at 100℃; for 6h; |
Conditions | Yield |
---|---|
With sodium hydroxide for 72h; Inert atmosphere; Reflux; | 99% |
With sodium hydroxide In water for 72h; Inert atmosphere; | 96.5% |
With potassium hydroxide In water for 24h; Reflux; | 90% |
Conditions | Yield |
---|---|
With thionyl chloride at 80℃; for 4h; Cooling with ice; Reflux; | 98.2% |
With thionyl chloride at 0℃; for 15h; Heating / reflux; | 92% |
With sulfuric acid for 20h; Reflux; Inert atmosphere; | 89% |
Conditions | Yield |
---|---|
With thionyl chloride at 0℃; for 48h; Heating / reflux; | 97% |
With sulfuric acid for 24h; Reflux; | 85% |
Conditions | Yield |
---|---|
Stage #1: pyrrolidine; 5-chloro-2-nitrobenzoic acid at 110℃; for 2h; Neat (no solvent); Stage #2: pH=Ca. 3; Acidic aq. solution; | 95.66% |
piperidine
5-chloro-2-nitrobenzoic acid
2-nitro-5-(piperidin-N-yl)-benzoic acid
Conditions | Yield |
---|---|
Stage #1: piperidine; 5-chloro-2-nitrobenzoic acid at 110℃; for 2h; Neat (no solvent); Stage #2: pH=Ca. 3; Acidic aq. solution; | 95.04% |
5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
With water-d2; silver carbonate In dimethyl sulfoxide at 120℃; for 16h; | 95% |
5-chloro-2-nitrobenzoic acid
5-dimethylamino-2-nitrobenzoic acid
Conditions | Yield |
---|---|
With dimethyl amine In water at 80℃; for 4h; | 94% |
Conditions | Yield |
---|---|
With copper(l) iodide; oxygen; copper(l) chloride In dimethyl sulfoxide at 160℃; under 760.051 Torr; for 30h; Schlenk technique; Sealed tube; | 93% |
With oxygen; silver carbonate; potassium hydroxide; copper dichloride In dimethyl sulfoxide; N,N-dimethyl-formamide at 130 - 140℃; | 80% |
With 2.9-dimethyl-1,10-phenanthroline; oxygen; copper (I) acetate; silver sulfate; sodium chloride In dimethyl sulfoxide at 160℃; for 24h; Schlenk technique; | 66% |
With 2.9-dimethyl-1,10-phenanthroline; oxygen; copper diacetate; silver sulfate; sodium chloride In dimethyl sulfoxide at 160℃; under 760.051 Torr; for 20h; Schlenk technique; | 64% |
5-chloro-2-nitrobenzoic acid
methyl iodide
methyl 5-chloro-2-nitrobenzoate
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 40℃; for 1h; | 92% |
With potassium carbonate In N,N-dimethyl-formamide at 0 - 40℃; for 1h; | 92% |
5-chloro-2-nitrobenzoic acid
1-iodo-5-chloro-2-nitrobenzene
Conditions | Yield |
---|---|
With copper(l) iodide; oxygen In dimethyl sulfoxide at 160℃; under 760.051 Torr; for 30h; Schlenk technique; Sealed tube; | 92% |
With 2.9-dimethyl-1,10-phenanthroline; oxygen; copper diacetate; silver sulfate; sodium iodide In dimethyl sulfoxide at 160℃; under 760.051 Torr; for 20h; Schlenk technique; | 76% |
iodobenzene
5-chloro-2-nitrobenzoic acid
5-chloro-2-nitro-1,1'-biphenyl
Conditions | Yield |
---|---|
With triphenylphosphine; silver carbonate; palladium dichloride In dimethyl sulfoxide; N,N-dimethyl-formamide at 130℃; for 30h; Inert atmosphere; | 92% |
5-chloro-2-nitrobenzoic acid
A
5-chloro-2-nitrobenzyl alcohol
B
5-(piperidin-1-yl)-2-nitrobenzaldehyde
Conditions | Yield |
---|---|
With hydrogenchloride In tetrahydrofuran | A 91% B n/a |
5-chloro-2-nitrobenzoic acid
dimethyl sulfate
5-methylthio-2-nitrobenzoic acid
Conditions | Yield |
---|---|
Stage #1: 5-chloro-2-nitrobenzoic acid With sodium sulfide nonahydrate; sodium hydroxide In water at 60℃; for 2.5h; Stage #2: dimethyl sulfate at 100℃; for 1h; | 90% |
With sodium sulfide; sodium hydroxide 1) water, 50-55 deg C, 2,5 h 2) reflux 1 h; Yield given. Multistep reaction; | |
Stage #1: 5-chloro-2-nitrobenzoic acid With sodium sulfide; sodium hydroxide at 60℃; Stage #2: dimethyl sulfate Heating; | |
Stage #1: 5-chloro-2-nitrobenzoic acid With sodium sulfide; sodium hydroxide In water at 60℃; for 2.5h; Stage #2: dimethyl sulfate With sodium hydroxide In water for 1h; Heating / reflux; Stage #3: With hydrogenchloride In water |
5-chloro-2-pyridylamine
5-chloro-2-nitrobenzoic acid
N-(5-chloropyridin-2-yl)-5-chloro-2-nitrobenzamide
Conditions | Yield |
---|---|
With pyridine; trichlorophosphate In acetonitrile at 0 - 30℃; for 1h; Inert atmosphere; | 90% |
With pyridine; trichlorophosphate at 20℃; for 0.0833333h; |
Conditions | Yield |
---|---|
With copper(l) iodide; triethylamine In dimethyl sulfoxide at 120℃; under 760.051 Torr; for 20h; Inert atmosphere; Schlenk technique; | 88% |
With 2.9-dimethyl-1,10-phenanthroline; oxygen; copper (I) acetate; silver sulfate; sodium iodide In dimethyl sulfoxide at 160℃; for 24h; Schlenk technique; | 76% |
With copper(I) oxide at 120℃; for 24h; Ionic liquid; |
Conditions | Yield |
---|---|
In tetrahydrofuran for 1h; Reflux; | 86% |
5-chloro-2-nitrobenzoic acid
5,5'-dichloro-2,2'-dinitro-1,1'-biphenyl
Conditions | Yield |
---|---|
With triphenylphosphine; silver carbonate; palladium dichloride In dimethyl sulfoxide at 130℃; for 6h; Inert atmosphere; | 85% |
With copper(l) iodide In dimethyl sulfoxide at 140℃; for 20h; Inert atmosphere; Molecular sieve; | 72% |
morpholine
5-chloro-2-nitrobenzoic acid
N-<5-chloro-2-nitrobenzoyl>morpholide
Conditions | Yield |
---|---|
In thionyl chloride; acetone | 84% |
In acetone at 0℃; for 0.25h; |
Cyclohexyl isocyanide
phenylglyoxal hydrate
5-chloro-2-nitrobenzoic acid
3-bromopropylamine hydrochloride
Conditions | Yield |
---|---|
Stage #1: Cyclohexyl isocyanide; phenylglyoxal hydrate; 5-chloro-2-nitrobenzoic acid; 3-bromopropylamine hydrochloride With sodium hydroxide In methanol at 20℃; for 24h; Stage #2: With caesium carbonate In methanol at 20℃; for 1h; | 84% |
5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
With potassium tert-butylate In ethanol at 20℃; | 83% |
5-chloro-2-nitrobenzoic acid
2,6-difluorobenzoic acid
A
2,2',6,6'-tetrafluoro-1,1'-biphenyl
B
5-chloro-2',6'-difluoro-2-nitro-1,1'-biphenyl
C
5,5'-dichloro-2,2'-dinitro-1,1'-biphenyl
Conditions | Yield |
---|---|
With triphenylphosphine; silver carbonate; palladium dichloride In dimethyl sulfoxide at 130℃; for 6h; Inert atmosphere; | A 11 %Chromat. B 79% C 21% |
5-chloro-2-nitrobenzoic acid
3-Amino-5-chloro-2-nitrobenzoic acid
Conditions | Yield |
---|---|
With O-Methylhydroxylamin; potassium tert-butylate; copper diacetate In 1,2-dimethoxyethane at 20℃; Substitution; Amination; | 78% |
With potassium tert-butylate; N-methoxylamine hydrochloride; copper diacetate In N,N-dimethyl-formamide at 0℃; for 3h; | 60.5% |
With potassium tert-butylate; N-methoxylamine hydrochloride; copper diacetate In N,N-dimethyl-formamide for 3h; | 32% |
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