4-Fluorobenzoic acid Product name: 4-Fluorobenzoic acid CAS: 456-22-4 Structural formula: Quality specification: Appearance: White powder Content: 98.0%/99.0%(HPLC)min Melting point: 182-184℃ As a professional manufacturer of fine chemicals, phar
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inquiryhigh quality Appearance:White or off white powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
4-Fluorobenzoic acid Product name: 4-Fluorobenzoic acid CAS: 456-22-4 Structural formula: Quality specification: Appearance: White powder Content: 98.0%/99.0%(HPLC)min Melting point: 182-184℃ Our Server 1. Competitive offers with s
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inquiryProduct Description Name 4-Fluorobenzoic acid CAS 456-22-4 Assay 99% Appearance
Cas:456-22-4
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inquiryAbout Product Details
Cas:456-22-4
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inquiryProduct Name: 4-Fluorobenzoic acid Synonyms: 4-FLUOROBENZOIC ACID;AKOS 92636;PFBA;P-FLUOROBENZOIC ACID;TIMTEC-BB SBB008568;RARECHEM AL BO 0053;4-fluoro-benzoicaci;Benzoic acid, p-fluoro- CAS:
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inquiryName:4-Fluorobenzoic acid CAS:456-22-4 Appearance:White Powder Application: 4-Fluorobenzoic acid is the intermediate of fluormorpholine, a fungicide. Appearance:White Powder Storage:Store in cool and dry place, away from sun ligh
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inquiry4-Fluorobenzoic acid Chemical Properties Melting point 182-184 °C (lit.) Boiling point 117 °C density 1.479 storage temp. Sealed in dry,Room Temperature solubility alcohol: soluble pka 4.15(at 25℃) form Crystalline
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inquiryConditions | Yield |
---|---|
With hydrogen bromide; dihydrogen peroxide at 50℃; for 9h; Temperature; UV-irradiation; | 96.8% |
With oxygen; Langlois reagent In acetonitrile at 25℃; for 12h; Irradiation; Green chemistry; | 96% |
With hydrogen bromide In water | 95.2% |
1,2-bis(4-fluorophenyl)-2-hydroxyethan-1-one
4-Fluorobenzoic acid
Conditions | Yield |
---|---|
With oxygen; sodium hydride In tetrahydrofuran; mineral oil at 25℃; under 760.051 Torr; for 0.5h; | 74% |
With diphenyl diselenide; dihydrogen peroxide In water; acetonitrile at 20℃; for 24h; | 72% |
Stage #1: 1,2-bis(4-fluorophenyl)-2-hydroxyethan-1-one With potassium cyanide; carbon dioxide In N,N-dimethyl-formamide at 12℃; under 760.051 Torr; for 1h; Stage #2: With titanium(IV)isopropoxide; 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide at 40℃; for 18h; Reagent/catalyst; | 10 %Spectr. |
Conditions | Yield |
---|---|
With 1,2-bis(diphenylphosphino)ethane nickel(II) chloride In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide Ambient temperature; electrochemically; | 94% |
Stage #1: 1-Bromo-4-fluorobenzene With bromobenzene; trifluoroacetic acid; cobalt(II) bromide; zinc dibromide; zinc In acetonitrile Inert atmosphere; Stage #2: carbon dioxide With palladium diacetate; tricyclohexylphosphine In tetrahydrofuran; acetonitrile at 0℃; under 760.051 Torr; Inert atmosphere; Stage #3: With hydrogenchloride In tetrahydrofuran; water; ethyl acetate; acetonitrile | 94% |
With (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; 2-(diphenylphosphino)-2’(3-(dimethylamino)-3-oxopropyl)-6’-(3-(icosyloxy)-3-oxopropyl)biphenyl; water; palladium diacetate; N-ethyl-N,N-diisopropylamine In toluene under 760.051 Torr; for 16h; Inert atmosphere; Schlenk technique; Irradiation; | 88% |
carbon dioxide
2-(4-fluorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane
4-Fluorobenzoic acid
Conditions | Yield |
---|---|
With (1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)imidazolidin-2-ylidene)copper(I) bromide; potassium tert-butylate In tetrahydrofuran under 760.051 Torr; for 24h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Reflux; Green chemistry; | 96% |
Stage #1: carbon dioxide; 2-(4-fluorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane With [Ni(N,N'-bis[2,6-bis(diphenylmethyl)-4-methylphenyl]imidazole-2-ylidene)(allyl)Cl]; potassium tert-butylate In toluene at 100℃; under 760.051 Torr; for 15h; Schlenk technique; Inert atmosphere; Stage #2: With hydrogenchloride In water; ethyl acetate; toluene at 20℃; | 96% |
With potassium tert-butylate; copper(l) chloride; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride In tetrahydrofuran at 70℃; under 760.051 Torr; for 24h; | 89% |
Conditions | Yield |
---|---|
With peracetic acid; C24H29INO5 In acetic acid at 30℃; for 48h; | A 67% B 19% |
With tert.-butylhydroperoxide In hexane; water at 50℃; for 9.5h; | A 62% B 22% |
With sodium hypochlorite; sodium hydrogencarbonate for 4h; Yield given. Yields of byproduct given; | |
With [Rh(III)(OEP)(Cl)]/C; sodium hydroxide In water at 25℃; Electrochemical reaction; Inert atmosphere; | |
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; C40H32B2Cu2F10N8S2*2CH4O; potassium carbonate In water at 40℃; under 760.051 Torr; for 24h; Green chemistry; |
Conditions | Yield |
---|---|
With C4H11FeMo6NO24(3-)*3C16H36N(1+); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 8h; Green chemistry; | 99% |
With 4H3N*4H(1+)*CuMo6O18(OH)6(4-); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 12h; | 99% |
With tert.-butylnitrite; N-hydroxyphthalimide; oxygen In water at 60℃; under 760.051 Torr; for 48h; Schlenk technique; | 99% |
Conditions | Yield |
---|---|
With sodium periodate; sulfuric acid In water at 95℃; for 12h; | 86% |
With tert.-butylhydroperoxide at 100℃; for 5h; | 80% |
With tert.-butylhydroperoxide In water at 80℃; for 12h; Green chemistry; | |
Multi-step reaction with 2 steps 1: silver(I) nitrite / diethyl ether / 5 h / 0 °C / Reflux 2: tetra-(n-butyl)ammonium iodide; zinc diacetate; water / 24 h / 80 °C View Scheme | |
Multi-step reaction with 2 steps 1.1: sodium hydride / tetrahydrofuran / 0.08 h / Inert atmosphere 1.2: 5 h / Inert atmosphere; Reflux 2.1: bis(acetylacetonate)oxovanadium; sodium acetate; methyl 3,5-bis((1H-1,2,4-triazol-1-yl)methyl)benzoate; oxygen / 48 h / 120 °C View Scheme |
potassium monomethylcarbonate
2-(4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
4-Fluorobenzoic acid
Conditions | Yield |
---|---|
With chloro[1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene]copper(I) In tetrahydrofuran at 70℃; for 16h; Inert atmosphere; Sealed tube; | 89% |
Conditions | Yield |
---|---|
With iodine; aluminium In acetonitrile at 80℃; for 18h; | 98% |
With high-silica Hβ-75 zeolite In water at 130℃; for 24h; Reagent/catalyst; | 75% |
Conditions | Yield |
---|---|
With water; potassium carbonate In acetonitrile at 100℃; under 3750.38 Torr; for 0.0161111h; | 96% |
With water; palladium diacetate; potassium carbonate at 20℃; under 760.051 Torr; for 5h; | 92% |
With water; sodium carbonate; palladium diacetate at 20 - 165℃; under 10501.1 - 22502.3 Torr; for 0.333333h; microwave irradiation; | 77% |
With 4,4’‐bis(trimethylammoniummethyl)‐2,2’‐bipyridine; bis-triphenylphosphine-palladium(II) chloride; water; sodium carbonate In water at 100℃; under 7600.51 Torr; for 24h; Catalytic behavior; Autoclave; | 74% |
4-Fluorobenzoic acid
Conditions | Yield |
---|---|
With ammonium cerium (IV) nitrate; oxygen In acetonitrile at 20 - 50℃; for 4h; | 89% |
Conditions | Yield |
---|---|
With sodium hypochlorite; sodium hydrogencarbonate for 1.33333h; | 100% |
With diethylene glycol dimethyl ether at 70℃; for 0.5h; Sonication; | 97% |
With oxygen at 120℃; for 10h; Green chemistry; | 95% |
Conditions | Yield |
---|---|
With 4 Angstroem MS; methyl tri-n-octyl ammonium hydrogen sulfate; sodium tungstate at 90℃; for 10h; | 86% |
With Oxone In water; acetonitrile for 12h; Reflux; | 85% |
Conditions | Yield |
---|---|
Stage #1: 1-(4-fluorophenyl)ethanone With tert.-butylhydroperoxide; sodium hydroxide; tungsten(VI) oxide In water at 80℃; for 8h; Stage #2: With hydrogenchloride In water | 93% |
Stage #1: 1-(4-fluorophenyl)ethanone With iodine; dimethyl sulfoxide In chlorobenzene at 130℃; for 3h; Stage #2: With tert.-butylhydroperoxide In chlorobenzene at 20 - 130℃; for 3h; | 93% |
With oxygen; manganese (II) acetate tetrahydrate; cobalt(II) diacetate tetrahydrate In acetic acid at 100℃; under 760.051 Torr; for 15h; | 88% |
Conditions | Yield |
---|---|
With copper(l) iodide; N,N,N,N,-tetramethylethylenediamine; diethylzinc In N,N-dimethyl acetamide at 70℃; under 760.051 Torr; | 60% |
Stage #1: 4-fluoro-1-iodobenzene With copper In tetrahydrofuran at 25℃; for 0.5h; Stage #2: carbon dioxide In tetrahydrofuran for 24h; | 42% |
Conditions | Yield |
---|---|
With copper(l) iodide; potassium carbonate In dimethyl sulfoxide at 100℃; for 24h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With chloro[1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene]copper(I); potassium methanolate In N,N-dimethyl acetamide at 70℃; for 24h; Schlenk technique; Sealed tube; | 73% |
Conditions | Yield |
---|---|
With 2.9-dimethyl-1,10-phenanthroline; neocuproine; zinc In dimethyl sulfoxide at 20℃; under 760.051 Torr; for 16h; | 74% |
carbon monoxide
1-Bromo-4-fluorobenzene
A
4-Fluorobenzoic acid
B
methyl 4-flurobenzoate
Conditions | Yield |
---|---|
With methanol; tert-Amyl alcohol; sodium hydride; cobalt(II) acetate In tetrahydrofuran at 40℃; under 760 Torr; for 7h; Irradiation; | A 8% B 81.5% |
1,2-bis(4-fluorophenyl)-1,2-ethanediol
4-Fluorobenzoic acid
Conditions | Yield |
---|---|
With oxygen In dichloromethane at 20℃; under 760.051 Torr; for 12h; Irradiation; | 88% |
Stage #1: 1,2-bis(4-fluorophenyl)-1,2-ethanediol With oxygen; sodium t-butanolate In tetrahydrofuran at 20℃; under 760.051 Torr; for 3h; Stage #2: With hydrogenchloride In tetrahydrofuran; water pH=1; chemoselective reaction; | 70% |
Conditions | Yield |
---|---|
Stage #1: para-fluorostyrene With tert.-butylhydroperoxide; iodine; sodium hydroxide In water at 105℃; for 16h; Sealed tube; Stage #2: With hydrogenchloride In water | 52% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 25℃; for 3.5h; Cannizzaro Reaction; | A n/a B 86% |
With potassium hydroxide | |
With barium dihydroxide; formaldehyd at 100 - 110℃; for 0.2h; | A 88 % Chromat. B 11 % Chromat. |
Stage #1: 4-fluorobenzaldehyde In neat (no solvent) for 0.0333333h; Green chemistry; Stage #2: With 1,4-diaza-bicyclo[2.2.2]octane In neat (no solvent) at 40℃; for 0.00416667h; Reagent/catalyst; Cannizzaro Reaction; Microwave irradiation; Green chemistry; |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; dicobalt octacarbonyl In sodium hydroxide; benzene at 65℃; for 2h; Irradiation; | 97% |
With dicobalt octacarbonyl; potassium carbonate; methyloxirane In methanol at 60℃; under 760 Torr; for 6h; | 89% |
carbon dioxide
4-fluorophenyl trifluoromethanesulfonate
4-Fluorobenzoic acid
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate; bis-triphenylphosphine-palladium(II) chloride In N,N-dimethyl-formamide at 90℃; electrochemical reaction; | 92% |
With (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; palladium diacetate; caesium carbonate; N-ethyl-N,N-diisopropylamine; DavePhos In N,N-dimethyl acetamide at 20℃; for 36h; Irradiation; Green chemistry; chemoselective reaction; | 62% |
With (2’,4’,6’-triisopropyl-[1,1’-biphenyl]-2-yl)-diphenylphosphine; bis(2-phenylpyridinato)(2,2'-bipyridine)iridium(III) hexafluorophosphate; tetrabutylammomium bromide; palladium diacetate; caesium carbonate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl acetamide at 20℃; under 760.051 Torr; for 4h; Irradiation; |
1-(4-Fluorophenyl)ethanol
A
4-Fluorobenzoic acid
B
1-(4-fluorophenyl)ethanone
Conditions | Yield |
---|---|
Stage #1: 1-(4-Fluorophenyl)ethanol With oxygen; sodium hydride In tetrahydrofuran at 0 - 20℃; for 6h; Stage #2: With hydrogenchloride In water | A 32% B 64% |
methyl 4-flurobenzoate
acetonitrile
A
4-Fluorobenzoic acid
B
3-(4-fluorophenyl)-3-oxopropionitrile
Conditions | Yield |
---|---|
With sodium hydride In tert-butyl methyl ether; water at 90℃; | A 17.5% B 64% |
N-(4-cyanophenyl)-4-fluorobenzamide
4-Fluorobenzoic acid
Conditions | Yield |
---|---|
With hydrogenchloride at 120℃; for 24h; | 98% |
Conditions | Yield |
---|---|
With aluminum tri-bromide; triisopropylsilyl chloride at 80℃; under 22502.3 Torr; for 48h; Autoclave; | 53% |
With aluminium trichloride; aluminium at 40℃; under 42754.3 Torr; for 18h; | 47% |
With triethylamine In acetonitrile at 20℃; under 760.051 Torr; for 24h; Irradiation; | 62 %Spectr. |
Conditions | Yield |
---|---|
Stage #1: carbon dioxide; 1-Chloro-4-fluorobenzene With manganese; bis(triphenylphosphine)nickel(II) chloride; tetraethylammonium iodide; triphenylphosphine In 1,3-dimethyl-2-imidazolidinone at 25℃; under 760.051 Torr; for 20h; Stage #2: With hydrogenchloride; water In diethyl ether at 20℃; for 0.166667h; | 81% |
With manganese; 2,9-dibutyl-4,7-dimethyl-1,10-phenanthroline; tetraethylammonium iodide; lithium acetate; cobalt(II) bromide In N,N-dimethyl acetamide at 100℃; under 760.051 Torr; for 12h; Inert atmosphere; Schlenk technique; | 62% |
Stage #1: 1-Chloro-4-fluorobenzene With bis(cyclopentadienyl)titanium dichloride; butyl magnesium bromide In tetrahydrofuran at 40℃; for 6h; Inert atmosphere; Schlenk technique; Stage #2: carbon dioxide In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; Schlenk technique; | 59% |
With tetrabutylammonium tetrafluoroborate In N,N-dimethyl-formamide at 20℃; under 760.051 Torr; for 4h; Electrolysis; | 51% |
Conditions | Yield |
---|---|
100% | |
With pyridine hydrogenfluoride; sodium nitrite 1.) O deg C, 20 min, 2.) 100 deg C, 1 h; | 89% |
With hydrogen fluoride; sodium nitrite |
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