B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In acetonitrile | A 100% B 99% |
A
pyridine
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In water addn. of KCl to C5H5NHBF4; extn. of pyridine with CHCl3, pptn., filtration, washing with a water-alcohol mixture, drying in a hot air oven (about 105°C), elem. anal.; | A n/a B 96% |
boron trifluoride
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane (N2); Schlenk technique; BF3 (5 equiv.) was introduced to stirred suspn.of K2(C6F4(BF3)2) in CH2Cl2 at -40°C; after 30 min soln. degasse d in vac. at -78°C; filtered; residue washed (CH2Cl2); solvent from filtrate distd. (vac.); | A 84% B n/a |
thallium(I) tetrafluoroborate
Potassium benzoate
C
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In tetrahydrofuran Ar atmosphere, stirring of Ni-complex and TlBF4 in THF (20°C, 2 h), removal of pptd. TlCl (filtn.), addn. of K-carboxylate, stirring (20°C, 2 h); removal of pptd. KBF4, partial evapn., pptn. on pentane addn., collection, washing (pentane), drying (vac.); elem. anal.; | A n/a B 78% C n/a |
cis-dichlorobis(diethylsulfide)platinum(II)
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With N(C2H5)3 In methanol stirred for 16 h; filtered, filtrate evapd., dissolved in CH2Cl2, dried in vac., crystn. (CH2Cl2-diethyl ether); elem. anal.; | A 78% B n/a |
With N(C2H5)3 In methanol stirred for 16 h; filtered, filtrate evapd., dissolved in CH2Cl2, addn. of H2O in a separating funnel, shaken, CH2Cl2-phase sepd., removal of solvent under reduced pressure, dried in vac., crystn. (CH2Cl2-diethyl ether); elem. anal.; | A 34% B n/a |
thallium(I) tetrafluoroborate
potassium 4-nitrobenzoate
C
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In tetrahydrofuran Ar atmosphere, stirring of Ni-complex and TlBF4 in THF (20°C, 2 h), removal of pptd. TlCl (filtn.), addn. of K-carboxylate, stirring (20°C, 2 h); removal of pptd. KBF4, partial evapn., pptn. on pentane addn., collection, washing (pentane), drying (vac.); elem. anal.; | A n/a B 68% C n/a |
thallium(I) tetrafluoroborate
potassium acetate
C
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In tetrahydrofuran Ar atmosphere, stirring of Ni-complex and TlBF4 in THF (20°C, 2 h), removal of pptd. TlCl (filtn.), addn. of K-carboxylate, stirring (20°C, 2 h); removal of pptd. KBF4, partial evapn., pptn. on pentane addn., collection, washing (pentane), drying (vac.); elem. anal.; | A n/a B 63% C n/a |
thallium(I) tetrafluoroborate
p-F-C6H4COOK
C
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In tetrahydrofuran Ar atmosphere, stirring of Ni-complex and TlBF4 in THF (20°C, 2 h), removal of pptd. TlCl (filtn.), addn. of K-carboxylate, stirring (20°C, 2 h); removal of pptd. KBF4, partial evapn., pptn. on pentane addn., collection, washing (pentane), drying (vac.); elem. anal.; | A n/a B 59% C n/a |
potassium iodide
A
{(pentacarbonyl)rhenium(ethylene)}BF4
B
rhenium pentacarbonyl iodide
C
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In tetrahydrofuran Rhenium-complex is suspended in THF under N2, addn. of KI, reaction mixture is stirred for 15 h at room temp.; light yellow soln. and a colourless ppt. are obtained, sepn. of ppt. and drying, removal of solvent of yellow soln., addn. of petrolether to resulting ppt., pptn. of (OC)5ReI, drying under vac., sublimation at 60°C, elem. anal.; | A n/a B 45% C n/a |
thallium(I) tetrafluoroborate
potassium acetate
C
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With tetrahydrofuran In tetrahydrofuran Ar atmosphere, stirring of Ni-complex and TlBF4 in THF (20°C, 2 h), removal of pptd. TlCl (filtn.), addn. of K-carboxylate, stirring (20°C, 2 h); removal of pptd. KBF4, partial evapn., pptn. on pentane addn., collection, washing (pentane), drying (vac.); elem. anal.; | A n/a B 42% C n/a |
[OsH(κ(2)-OCOCH3)(CCH2CMe3)(PiPr3)2]BF4
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In methanol stirring (room temp., 5 min), evapn., pptn. on toluene addn.; filtering, evapn., pptn. on MeOH addn., washing (MeOH), drying (vac.); elem. anal.; | A 40% B n/a |
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In methanol stirring (room temp., 5 min), evapn., pptn. on toluene addn.; filtering, evapn., pptn. on MeOH addn., washing (MeOH), drying (vac.); elem. anal.; | A 23% B n/a |
Conditions | Yield |
---|---|
With hydrogen fluoride; boron trifluoride at 20℃; Product distribution / selectivity; |
potassium hydrogenfluoride
Trimethyl borate
A
potassium tetrafluoroborate
B
potassium methoxytrifluoroborate
Conditions | Yield |
---|---|
In methanol; water KHF2 dissolved in aq. MeOH, B(OMe)3 added by stirring; after 1 h decanted, pptd. dissolved in water allowed to stand 4 d, detected by 19F NMR spectra; final molar ratio of (BF3OMe)(1-) to (BF4)(1-) 96:1; |
2-methylphenyl diazonium tetrafluoroborate
potassium thioacyanate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; dimethyl sulfoxide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 2-MeC6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.) , Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMSO (1:4)for 45 min; evolution of gas at 10-15°C for 1 h; | |
With 2-MeC6H4CH2CH(SCN)CONHCH2NHCOCHCH2; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 2-MeC6H4N2BF4 to 2-MeC6H4CH2CH(SCN)CONHCH2NHCOCHCH2, Cu(BF4)2*6H2O and KSCN in H2O-DMF (1:3) for 20 min; evolution of gas at 15-20°C for 45 min; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 2-MeC6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.) , Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMF (1:3) for 45 min; evolution of gas at 10-15°C for 1 h; |
K(1+)*HRu3(1-)*11CO=K(HRu3(CO)11)
trityl tetrafluoroborate
A
dodecacarbonyl-triangulo-triruthenium
B
triphenylmethane
C
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With carbon monoxide In tetrahydrofuran react. K(HRu3(CO)11) and (Ph3C)(BF4) in THF with CO (1 atm) at room temp. for 30 min; |
Conditions | Yield |
---|---|
In water | |
In water |
Conditions | Yield |
---|---|
byproducts: H2O; | |
byproducts: H2O; |
boric acid
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With potassium fluoride byproducts: H2O; | |
With potassium hydroxide; hydrogen fluoride In not given | |
With KF byproducts: H2O; |
1,4-Butanediol diacrylate
potassium thioacyanate
benzenediazonium tetrafluoroborate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
copper(II) bis(tetrafluoroborate) In water; acetone addn. of PhN2BF4 to soln. of 1,4-bis(acryloyloxy)butane, Cu(BF4)2 and KSCN in aq. acetone (1:2) for 45-60 min; cooling at -10 - -5°C for 2 h; evolution of N2; treatment of residual with Et2O, extn., washing with water, drying with MgSO4, removal of ether, chromy.; |
1,4-Butanediol diacrylate
potassium thioacyanate
4-nitrobenzenediazonium tetrafluoroborate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
copper(II) bis(tetrafluoroborate) In water; acetone addn. of NO2C6H4N2BF4 to soln. of 1,4-bis(acryloyloxy)butane, Cu(BF4)2 and KSCN in aq. acetone (1:2) for 45-60 min; cooling at -10 - -5°Cfor 2 h; evolution of N2; treatment of residual with Et2O, extn., washing with water, drying with MgSO4, removal of ether, chromy.; |
1,4-Butanediol diacrylate
potassium thioacyanate
4-methylbenzenediazonium tetrafluoroborate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
copper(II) bis(tetrafluoroborate) In water; acetone addn. of CH3C6H4N2BF4 to 1,4-bis(acryloyloxy)butane, Cu(BF4)2 and KSCN in aq. acetone (1:2) for 45-60 min; cooling at -10 - -5°C for 2 h; evolution of N2, treatment of residual with Et2O, extn., washing with water, drying with MgSO4, removal of ether, chromy.; |
Conditions | Yield |
---|---|
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: Cl2C6H3CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H3Cl2; addn. of 2,5-Cl2C6H3N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMF (1:3) for 45 min; evolution of gas at 10-15°C for 1 h; | |
With 2,5-Cl2C6H3CH2CH(SCN)CONHCH2NHCOCHCH2; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: Cl2C6H3CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H3Cl2; addn. of 2,5-Cl2C6H3N2BF4 to 2,5-Cl2C6H3CH2CH(SCN)CONHCH2NHCOCHCH2, Cu(BF4)2*6H2O and KSCN in H2O-DMF (1:3) for 20 min; evolution of gas at 15-20°C for 45 min; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; dimethyl sulfoxide byproducts: Cl2C6H3CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H3Cl2; addn. of 2,5-Cl2C6H3N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.) , Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMSO (1:4) for 45 min; evolution of gas at 10-15°C for 1 h; |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With KCl byproducts: NOCl; |
4-methoxybenzenediazonium tetrafluoroborate
potassium thioacyanate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With 4-MeOC6H4CH2CH(SCN)CONHCH2NHCOCHCH2; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: MeOC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4OMe; addn. of 4-MeOC6H4N2BF4 to 4-MeOC6H4CH2CH(SCN)CONHCH2NHCOCHCH2, Cu(BF4)2*6H2O and KSCN in H2O-DMF (1:3) for 20 min; evolution of gas at 15-20°C for 45 min; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; dimethyl sulfoxide byproducts: MeOC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4OMe; addn. of 4-MeOC6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMSO (1:4)for 45 min; evolution of gas at 10-15°C for 1 h; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: MeOC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4OMe; addn. of 4-MeOC6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMF (1:3) for 45 min; evolution of gas at 10-15°C for 1 h; |
potassium thioacyanate
benzenediazonium tetrafluoroborate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; dimethyl sulfoxide byproducts: C6H5CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H5; addn. of PhN2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMSO (1:4) for 45min; evolution of gas at 10-15°C for 1 h; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: C6H5CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H5; addn. of PhN2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMF (1:3) for 45 min; evolution of gas at 10-15°C for 1 h; | |
With PhCH2CH(SCN)CONHCH2NHCOCHCH2; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: C6H5CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H5; addn. of PhN2BF4 to PhCH2CH(SCN)CONHCH2NHCOCHCH2, Cu(BF4)2*6H2O and KSCN in H2O-DMF (1:3) for 20 min; evolution of gas at 15-20°C for 45 min; |
potassium thioacyanate
4-nitrobenzenediazonium tetrafluoroborate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With 4-NO2C6H4CH2CH(SCN)CONHCH2NHCOCHCH2; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: NO2C6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4NO2; addn. of 4-NO2C6H4N2BF4 to 4-NO2C6H4CH2CH(SCN)CONHCH2NHCOCHCH2, Cu(BF4)2*6H2O and KSCN in H2O-DMF (1:3) for 20 min; evolution of gas at 15-20°C for 45 min; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; dimethyl sulfoxide byproducts: NO2C6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4NO2; addn. of 4-NO2C6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMSO (1:4)for 45 min; evolution of gas at 10-15°C for 1 h; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: NO2C6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4NO2; addn. of 4-NO2C6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMF (1:3) for 45 min; evolution of gas at 10-15°C for 1 h; |
potassium thioacyanate
4-methylbenzenediazonium tetrafluoroborate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; dimethyl sulfoxide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 4-MeC6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMSO (1:4) for 45 min; evolution of gas at 10-15°C for 1 h; | |
With 4-MeC6H4CH3CH(SCN)CONHCH2NHCOCHCH2; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 4-MeC6H4N2BF4 to 4-MeC6H4CH2CH(SCN)CONHCH2NHCOCHCH2, Cu(BF4)2*6H2O and KSCN in H2O-DMF (1:3) for 20 min; evolution of gas at 15-20°C for 45 min; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 4-MeC6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.) , Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMF (1:3) for 45 min; evolution of gas at 10-15°C for 1 h; |
potassium thioacyanate
3-methylbenzenediazonium tetrafluoroborate
A
nitrogen
B
potassium tetrafluoroborate
Conditions | Yield |
---|---|
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; dimethyl sulfoxide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 3-MeC6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.), Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMSO (1:4) for 45 min; evolution of gas at 10-15°C for 1 h; | |
With 3-MeC6H4CH2CH(SCN)CONHCH2NHCOCHCH2; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 3-MeC6H4N2BF4 to 3-MeC6H4CH2CH(SCN)CONHCH2NHCOCHCH2, Cu(BF4)2*6H2O and KSCN in H2O-DMF (1:3) for 20 min; evolution of gas at 15-20°C for 45 min; | |
With N,N-methylenediacrylamide; copper(II) tetrafluroborate hexahydrate In water; N,N-dimethyl-formamide byproducts: MeC6H4CH2CH(SCN)CONHCH2NHCOCH(SCN)CH2C6H4Me; addn. of 3-MeC6H4N2BF4 (2.2 equiv.) to N,N-methylenediacrylamide (1 equiv.) , Cu(BF4)2*6H2O (0.1 equiv.) and KSCN (1.1 equiv.) in H2O-DMF (1:3) for 45 min; evolution of gas at 10-15°C for 1 h; |
hydrogen fluoride
boric acid
potassium carbonate
potassium tetrafluoroborate
1-methyl-1H-imidazole
potassium tetrafluoroborate
Conditions | Yield |
---|---|
Stage #1: 1-methyl-1H-imidazole; 4-(chloromethyl)benzyl 3-O-acetyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside In acetonitrile at 85℃; for 24h; Inert atmosphere; Stage #2: potassium tetrafluoroborate In acetonitrile at 85℃; for 24h; Inert atmosphere; | 100% |
water
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In methanol 10-fold excess of KBF4; elem. anal., XRD; | 99% |
Conditions | Yield |
---|---|
In methanol 10-fold excess of KBF4; elem. anal.; | 99% |
Conditions | Yield |
---|---|
In methanol 10-fold excess of KBF4; elem. anal.; | 99% |
Conditions | Yield |
---|---|
In methanol 10-fold excess of KBF4; elem. anal., XRD; | 99% |
Conditions | Yield |
---|---|
In methanol 10-fold excess of KBF4; elem. anal., XRD; | 99% |
Conditions | Yield |
---|---|
In methanol 10-fold excess of KBF4; elem. anal., XRD; | 99% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In methanol 10-fold excess of KBF4; elem. anal., XRD; | 99% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; Inert atmosphere; | 99% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; Inert atmosphere; | 99% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; Inert atmosphere; | 98% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; Inert atmosphere; | 96% |
tetrabutylammomium bromide
potassium tetrafluoroborate
tetrabutylammonium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; for 24h; | 96% |
In dichloromethane; water at 25℃; for 24h; | 96% |
In dichloromethane; water at 20℃; for 24h; | 96% |
In dichloromethane; water at 20℃; for 24h; | 96% |
trimethylsilyl cyanide
potassium tetrafluoroborate
potassium monofluorotricyanoborate
Conditions | Yield |
---|---|
With gallium(III) trichloride for 6h; Reflux; | 96% |
With chloro-trimethyl-silane In 1,2-dimethoxyethane at 75℃; for 7h; Inert atmosphere; | 85.2% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane | 96% |
Conditions | Yield |
---|---|
at 48 - 52℃; for 6h; Inert atmosphere; | 95.2% |
tetraoctyl ammonium bromide
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; for 24h; | 95% |
Conditions | Yield |
---|---|
In methanol; water for 24h; Schlenk technique; Inert atmosphere; | 95% |
tetrakis(acetonitrile)palladium(II) tetrafluoroborate
potassium tetrafluoroborate
Conditions | Yield |
---|---|
Stage #1: tetrakis(acetonitrile)palladium(II) tetrafluoroborate; C60H50IrN6(1+)*BF4(1-) In dimethylsulfoxide-d6 at 85℃; for 12h; Inert atmosphere; Schlenk technique; Stage #2: potassium tetrafluoroborate In methanol; dimethylsulfoxide-d6; water at 20℃; for 4h; Inert atmosphere; Schlenk technique; | 95% |
tetrakis(acetonitrile)palladium(II) tetrafluoroborate
potassium tetrafluoroborate
Conditions | Yield |
---|---|
Stage #1: tetrakis(acetonitrile)palladium(II) tetrafluoroborate; C60H50IrN6(1+)*BF4(1-) In dimethylsulfoxide-d6 at 85℃; for 12h; Inert atmosphere; Schlenk technique; Stage #2: potassium tetrafluoroborate In methanol; dimethylsulfoxide-d6; water at 20℃; for 4h; Inert atmosphere; Schlenk technique; | 95% |
potassium tetrafluoroborate
N-benzyl-N,N-diethylethanaminium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; for 24h; | 95% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 68 - 72℃; for 12h; Inert atmosphere; | 94.8% |
potassium tetrafluoroborate
A
tris[triphenylphosphinegold(I)]oxonium tetrafluoroborate
B
potassium 2-nitrophenoxide
Conditions | Yield |
---|---|
In toluene byproducts: potassium o-nitrophenoxide; addn. of H2O and KBF4 to soln. of Au-complex (stirring 20 min); ppt. sepn., repptn. from CHCl3 by ether; | A 94% B 91% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
In methanol; water for 24h; Schlenk technique; Inert atmosphere; | 94% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In acetonitrile at 100℃; for 0.166667h; | 94% |
trimethylsilyl cyanide
potassium tetrafluoroborate
B
potassium monofluorotricyanoborate
Conditions | Yield |
---|---|
With gallium(III) trichloride for 15h; Time; Reflux; | A 7% B 93% |
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In water at 20℃; for 48h; | 92% |
Product Name: Potassium tetrafluoroborate (CAS NO.14075-53-7)
Molecular Formula: KBF4
Molecular Weight: 125.90g/mol
Mol File: 14075-53-7.mol
EINECS: 237-928-2
Appearance: white odourlesss crystalline powder
Melting Point: 530 °C(lit.)
Refractive index: 1.3245
Water Solubility: 4.4 g/L (20 °C)
Sensitive: Moisture Sensitive
Stability: Stable. May decompose on exposure to water or moisture. Incompatible with metals.
H-Bond Donor: 0
H-Bond Acceptor: 5
Structure Descriptors of Potassium tetrafluoroborate (CAS NO.14075-53-7):
IUPAC Name: potassium tetrafluoroborate
Canonical SMILES: [B-](F)(F)(F)F.[K+]
InChI: InChI=1S/BF4.K/c2-1(3,4)5;/q-1;+1
InChIKey: AKEBROIVCDHVSD-UHFFFAOYSA-N
Product Categories: Inorganic Chemicals; Inorganics
Potassium tetrafluoroborate (CAS NO.14075-53-7) is used in metallurgical industry and maked three fluorinated boron
and other Fluorinated salt raw materials, etc.
1. | ipr-rat LD50:240 mg/kg | 14KTAK Boron, Metallo-Boron Compounds and Boranes R.M. Adams,New York, NY.: Wiley,1964,693. | ||
2. | ipr-mus LD50:590 mg/kg | 14KTAK Boron, Metallo-Boron Compounds and Boranes R.M. Adams,New York, NY.: Wiley,1964,693. | ||
3. | ipr-rbt LD50:380 mg/kg | 14KTAK Boron, Metallo-Boron Compounds and Boranes R.M. Adams,New York, NY.: Wiley,1964,693. |
Reported in EPA TSCA Inventory.
Poison by intraperitoneal route. When heated to decomposition it emits very toxic fumes of F−, K2O, and BOx. Used in sand casting of aluminum and magnesium, grinding, and in resinoid grinding wheels. See also FLUORIDES and BORON COMPOUNDS.
Safety Information of Potassium tetrafluoroborate (CAS NO.14075-53-7):
Hazard Codes: Xi,C
Risk Statements: 36/37/38-34
R36/37/38:Irritating to eyes, respiratory system and skin.
R34:Causes burns.
Safety Statements: 37/39-26-45-36/37/39
S37/39:Wear suitable gloves and eye/face protection.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
OSHA PEL: TWA 2.5 mg(F)/m3
ACGIH TLV: TWA 2.5 mg(F)/m3; BEI: 3 mg/g creatinine of fluorides in urine prior to shift; 10 mg/g creatinine of fluorides in urine at end of shift.
NIOSH REL: TWA (Inorganic Fluorides) 2.5 mg(F)/m3
Potassium tetrafluoroborate , its CAS NO. is 14075-53-7, the synonyms are Potassium tetrafluoroborate(1-) ; Borate(1-), tetrafluoro-, potassium ; Avogadrite ; Boron potassium fluoride .
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