Conditions | Yield |
---|---|
In dichloromethane at 26℃; Equilibrium constant; 9.1 - 10.6 M-1; |
C6H5O(1-)*C6H6O*C32H68N(1+)
benzyl bromide
A
(benzyloxy)benzene
B
tetraoctyl ammonium bromide
C
phenol
Conditions | Yield |
---|---|
In acetonitrile at 20℃; |
(η6-1-fluoro-3-methylbenzene)tricarbonylchromium(0)
tetraoctyl ammonium bromide
acetone oxime
(CO)3CrC6H4(CH3)ONC(CH3)2
Conditions | Yield |
---|---|
With potassium hydroxide In benzene (N2), stirred for 1 h; solvent removed under vac., residue dissolved in Et2O, filtered on Celite, evaporated, crystd. from di-isopropyl ether; | 98% |
propyl methanesulfonate
tetraoctyl ammonium bromide
A
propyl bromide
B
tetraoctylammonium methanesulfonate
Conditions | Yield |
---|---|
In benzene at 80℃; | A n/a B 97% |
potassium thioacyanate
tetraoctyl ammonium bromide
tetra-n-octylammonium thiocyanate
Conditions | Yield |
---|---|
In dichloromethane; water | 97% |
tetraoctyl ammonium bromide
bis(trifluoromethane)sulfonimide lithium
Conditions | Yield |
---|---|
In water; acetone at 20℃; for 12h; | 96% |
In water; acetone for 24h; | 89% |
In water at 20 - 70℃; for 73h; |
sodium dodecyl-sulfate
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
In water; acetone at 25℃; for 168h; | 95% |
tetraoctyl ammonium bromide
bis(tetra-n-octylammonium)hexachloridoplatinum(IV)
Conditions | Yield |
---|---|
In dichloromethane; water soln. of the bromide in CH2Cl2 added to soln. of K2PtCl6 in H2O; resulting two-phase system stirred at room temp. until complete decoloration of the aq. layer (3-5 h); organic layer sepd. and dried over MgSO4; solvent distilled off; elem. anal.; | 95% |
[Pd(1-diphenylphosphino-2-di-tert-butylphosphinoethylferrocene)(P(o-tolyl)3)]
toluene-4-sulfonic acid phenyl ester
tetraoctyl ammonium bromide
(C5H5)Fe(C5H3(P(C6H5)2)CH(CH3)P(C(CH3)3)2)Pd(C6H5)Br
Conditions | Yield |
---|---|
In benzene room temp., 9 h; | 95% |
In tetrahydrofuran Kinetics; |
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
With potassium tetrafluoroborate In dichloromethane; water at 20℃; for 24h; | 95% |
With potassium tetrafluoroborate In dichloromethane; water at 20℃; for 24h; | 95% |
2-iodophenylamine
tetraoctyl ammonium bromide
2-heptyl-1H-benzothiazole
Conditions | Yield |
---|---|
With sulfur; potassium hydroxide In water at 140℃; for 14h; Green chemistry; | 95% |
tetraoctyl ammonium bromide
potassium tetrafluoroborate
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; for 24h; | 95% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 70℃; Heating; | 95% |
Conditions | Yield |
---|---|
Stage #1: Au24Pt(SCH2CH2Ph)18 With sodium tetrahydroborate In tetrahydrofuran; ethanol for 0.5h; Stage #2: tetraoctyl ammonium bromide In tetrahydrofuran; methanol; ethanol | 95% |
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
Stage #1: 1,1,1-trifluoro-N-(pyridin-4(1H)-ylidene)methanesulfonamide With methanol; sodium at 20℃; for 1h; Inert atmosphere; Stage #2: tetraoctyl ammonium bromide for 14h; Inert atmosphere; | 95% |
lithium aluminium tetrahydride
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
at 50℃; for 4.66667h; Inert atmosphere; Reflux; | 94.9% |
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
Stage #1: tetraoctyl ammonium bromide; sodium dodecylbenzenesulfonate In water; acetone at 20℃; for 0.75h; Stage #2: In dichloromethane; water for 0.25h; | 94.2% |
[Pd(1-dicyclohexylphosphino-2-di-tert-butylphosphinoethylferrocene)(P(o-tolyl)3)]
toluene-4-sulfonic acid phenyl ester
tetraoctyl ammonium bromide
(C5H5)Fe(C5H3(P(C6H11)2)CH(CH3)P(C(CH3)3)2)Pd(C6H5)Br
Conditions | Yield |
---|---|
In benzene room temp., 5 min; | 94% |
Conditions | Yield |
---|---|
In propan-1-ol; water at 20℃; | 91% |
RhI(tetraphenylporphyrin)
tetraoctyl ammonium bromide
[Rh(5,10,15,20-tetraphenylporphyrinato)(n-octyl)]
Conditions | Yield |
---|---|
With sodium hydroxide In water; benzene at 120℃; for 5h; Sealed tube; | 91% |
tricarbonyl(η(6)-4-fluorotoluene)chromium
tetraoctyl ammonium bromide
acetone oxime
(CO)3CrC6H4(CH3)ONC(CH3)2
Conditions | Yield |
---|---|
With potassium hydroxide In benzene (N2), stirred for 3.5 h; solvent removed under vac., residue dissolved in Et2O, filtered on Celite, evaporated, crystd. from di-isopropyl ether; | 89% |
1,1,2,2-tetrafluoro-2-(phenylsulfanyl)ethanesulfonyl fluoride
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
Stage #1: 1,1,2,2-tetrafluoro-2-(phenylsulfanyl)ethanesulfonyl fluoride With lithium hydroxide monohydrate In diethyl ether at 20℃; Stage #2: tetraoctyl ammonium bromide In acetone at 20℃; for 0.0833333h; Inert atmosphere; | 89% |
tetraoctyl ammonium bromide
4-Fluoronitrobenzene
1-nitro-4-octyloxybenzene
Conditions | Yield |
---|---|
With water; copper(II) acetate monohydrate; caesium carbonate; Triphenylphosphine oxide at 145℃; Inert atmosphere; | 86% |
tetraoctyl ammonium bromide
bis(tetra-n-octylammonium)hexachloridoplatinum(IV)
Conditions | Yield |
---|---|
In propan-1-ol; water at 20℃; | 86% |
(η6-fluorobenzene)tricarbonylchromium
tetraoctyl ammonium bromide
acetone oxime
(CO)3CrC6H5ONC(CH3)2
Conditions | Yield |
---|---|
With potassium hydroxide In benzene (N2), stirred for 0.5 h; solvent removed under vac., residue dissolved in Et2O, filtered on Celite, evaporated, crystd. from di-isopropyl ether; | 85% |
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
In dichloromethane; water byproducts: NaBr; addn. of CH2Cl2 soln. of ammonium compound to aq. soln. of Au compound with vigorous stirring, 3 h; separation of phases, washing of organic phase (H2O), removement of solvent (room temp., vacuum), dissolution (CH2Cl2), filtration, evapn. (vacuum), pptn. (pentane), drying (vacuum, overnight); elem. anal.; | 85% |
sodium molybdate dihydrate
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
In hydrogenchloride; water soln. of NH4VO3 (0.11 mmol) in 37% HCl added to aq. soln. of Na2MoO4*2H2O (1.2 mmol); stirred (30 min, room temp.); (CH3(CH2)7)4NBr (0.4 mmol) added; ppt. filtered; washed with H2O and EtOH; dried in air; dissolved in CH3CN; crystd. (4°C, 24 h); crystals collected; washed with H2O and EtOH; dried in air; elem. anal.; | 85% |
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
Stage #1: sodium mid-chain branched dodecyl sulfate; tetraoctyl ammonium bromide In water; acetone at 20℃; for 0.75h; Stage #2: In dichloromethane; water for 0.25h; | 84.1% |
tricarbonyl(p-methoxychlorobenzene)chromium
tetraoctyl ammonium bromide
acetone oxime
Conditions | Yield |
---|---|
With potassium hydroxide In benzene (N2), stirred for 1.75 h; solvent removed under vac., residue dissolved in Et2O, filtered on Celite, evaporated, crystd. from di-isopropyl ether; | 84% |
1-methyl-1H-imidazole
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
In tetrahydrofuran for 72h; Reflux; | 79.6% |
gold(III) chloride hydrate
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
In propan-1-ol; water at 20℃; | 77% |
tetraoctyl ammonium bromide
Conditions | Yield |
---|---|
Stage #1: K8[α-SiW11O39]*13H2O; iron(III) chloride hexahydrate In water at 55℃; for 1.5h; pH=5; Stage #2: tetraoctyl ammonium bromide In water; toluene at 20℃; | 76% |
IUPAC Name : Betraoctylazanium bromide
Molecular Formula : C32H68BrN
EINECS : 238-936-9
Melting Point : 95 - 98 °C
Polar Surface Area: 0 Å2
Molecular Weight : 322.38 g/mol
Freely Rotating Bonds : 28
The Cas Register Number of Tetraoctyl ammonium bromide is 14866-33-2.The chemical synonyms of Tetraoctyl ammonium bromide (CAS NO.14866-33-2) are 1-octanaminium, N,N,N-trioctyl-, bromide ; 1-Octanaminium, N,N,N-trioctyl-, bromide (1:1) ; N,N,N-Trioctyl-1-octanaminium bromide ; N,N,N-Trioctyloctan-1-aminium bromide ; 14866-33-2 [RN] ; ammonium compounds, quaternary, tetraoctyl-, bromide ; tetra-N-Octylammonium bromide ; Tetraoctyl ammonium bromide .The molecular structure of Tetraoctyl ammonium bromide (CAS NO.14866-33-2) is.
Tetraoctyl ammonium bromide (CAS NO.14866-33-2) can be used in organic synthesis.
The extinguishing agent of Tetraoctyl ammonium bromide (CAS NO. 14866-33-2) are dry powder, foam, sand, carbon dioxide, water mist.
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