Conditions | Yield |
---|---|
In acetonitrile Reflux; Inert atmosphere; | 84% |
for 48h; Ambient temperature; | 81% |
at 20℃; for 43h; | 32% |
1-ethylpyridinium bromide
methyl trifluoromethanesulfonate
N-ethylpyridinium trifluoromethanesulfonate
Conditions | Yield |
---|---|
at 20℃; for 0.5h; Product distribution / selectivity; | 100% |
at 20℃; for 0.5h; | 100% |
trimethylsilyl trifluoromethanesulfonate
1-ethylpyridinium bromide
N-ethylpyridinium trifluoromethanesulfonate
Conditions | Yield |
---|---|
at 20℃; for 4h; Product distribution / selectivity; | 100% |
at 20℃; for 4h; | 100% |
Conditions | Yield |
---|---|
at 20℃; for 1h; | 100% |
1-ethylpyridinium bromide
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 24h; | 96% |
Conditions | Yield |
---|---|
With hydrogen bromide In water at 20℃; | 93% |
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 168h; | 89% |
In acetonitrile at 25℃; for 168h; | 89% |
1-ethylpyridinium bromide
1-ethylpyridinium 4',5'-dicyano-1,2,3-triazolate
Conditions | Yield |
---|---|
In methanol at 20℃; for 1h; | 86% |
1-ethylpyridinium bromide
Conditions | Yield |
---|---|
In acetonitrile at 25℃; for 168h; | 85% |
1-ethylpyridinium bromide
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 96h; | 84% |
sodium docusate
1-ethylpyridinium bromide
1-ethylpyridinium bis(2-ethylhexyl)sulfosuccinate
Conditions | Yield |
---|---|
In acetone; acetonitrile at 20℃; | 82% |
Conditions | Yield |
---|---|
With hydrogen bromide In water at 20℃; | 79% |
1-ethylpyridinium bromide
Conditions | Yield |
---|---|
With tellurium oxide; hydrogen bromide at 70℃; for 0.5h; | 79% |
1-ethylpyridinium bromide
Conditions | Yield |
---|---|
In acetonitrile for 11h; Ambient temperature; | 63% |
Conditions | Yield |
---|---|
Stage #1: C48H36NiO4S4(1-) In dichloromethane at 20℃; for 1h; Stage #2: 1-ethylpyridinium bromide In dichloromethane at 20℃; for 7h; | 53.6% |
1-ethylpyridinium bromide
Conditions | Yield |
---|---|
In acetonitrile | 46% |
N-methyl-4-methylpyridinium iodide
1-ethylpyridinium bromide
p-phenylpyridine
Conditions | Yield |
---|---|
With methylammonium sulfite; methylamine In water at 230℃; for 60h; | 37% |
Conditions | Yield |
---|---|
In methanol at 190℃; for 168h; Autoclave; | 20.9% |
Conditions | Yield |
---|---|
With hydrazine hydrate In methanol at 190℃; for 168h; Autoclave; | 14.1% |
1-ethylpyridinium bromide
1-ethyl-2-pyridone
Conditions | Yield |
---|---|
With water; sodium perbenzoate |
1-ethylpyridinium bromide
1-(3-hydroxy-2-phenylpropyl)pyridinium bromide
Conditions | Yield |
---|---|
With sodium hydroxide; benzaldehyde isomer(ic) I; | |
With sodium hydroxide; benzaldehyde isomer(ic) II; |
5-nitroindane-1,3-dione
1-ethylpyridinium bromide
2-(1-Ethyl-1H-pyridin-4-ylidene)-5-nitro-indan-1,3-dione
Conditions | Yield |
---|---|
With sodium hydroxide; air; oxygen 1.) MeOH, r.t., 8 d; Yield given. Multistep reaction; |
aluminium trichloride
1-ethylpyridinium bromide
N-ethylpyridinum tetrachloroaluminate
Conditions | Yield |
---|---|
In toluene (C7H10)Br and AlCl3 are reacted in toluene, react. yields toluene "liquid clathrate".; Crystn. by cooling toluene "liquid clathrate" at 258 K overnight.; |
Conditions | Yield |
---|---|
In diethyl ether reaction of borane with C6H5MgBr; 20 min at room temp. and subsequent treatment of the reaction product with 1-ethylpyridinium bromide; | |
In diethyl ether reaction of borane with C6H5MgBr; 20 min at room temp. and subsequent treatment of the reaction product with 1-ethylpyridinium bromide; |
potassium tetrakis(1-pyrrolyl)borate
1-ethylpyridinium bromide
tetrakis-phenylethynyl-boric acid ; ammonium salt
1-ethylpyridinium bromide
{C5H5NC2H5}(1+)*{B(CCC6H5)4}(1-)={C5H5NC2H5}{B(CCC6H5)4}
Conditions | Yield |
---|---|
In not given | |
In not given |
silver trifluoromethanesulfonate
1-ethylpyridinium bromide
N-ethylpyridinium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In water at 25℃; for 3h; |
1-ethylpyridinium bromide
Conditions | Yield |
---|---|
With tetrafluoroboric acid; silver(l) oxide In water Darkness; |
1-ethylpyridinium bromide
bis(trifluoromethanesulfonyl)amide
Conditions | Yield |
---|---|
In water at 20℃; for 3h; | |
In water at 20℃; for 3h; |
Molecular Structure:
Molecular Formula: C7H10BrN
Molecular Weight: 188.065
IUPAC Name: 1-Ethylpyridin-1-ium bromide
Synonyms of 1-Ethylpyridinium bromide (CAS NO.1906-79-2): AI3-52378 ; EINECS 217-607-3 ; Pyridinium, 1-ethyl-, bromide ; Pyridinium, 1-ethyl-, bromide (1:1)
CAS NO: 1906-79-2
Product Categories: Ionic Liquids ; Pyridinium Compounds ; Pyridinium Compounds (Ionic Liquids) ; Synthetic Organic Chemistry
Melting point: 117-121 °C
Hazard Codes of 1-Ethylpyridinium bromide (CAS NO.1906-79-2): Xi
Risk Statements: 36/37/38
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 37/39-26
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.
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