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inquiryProduct Description Product website: http://www.finerchem.com Product Name N,N-Dimethyldecylamine CAS No.
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N,N-dimethyldecanamide
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
With tris(pentafluorophenyl)borate; [Ru(1,1,1-tris(di(3,5-dimethoxyphenyl)phosphino-methyl)ethane)(trimethylenemethane)]; hydrogen In tetrahydrofuran at 160℃; under 75007.5 Torr; for 16h; | 97% |
With 9-borabicyclo[3.3.1]nonane In tetrahydrofuran at 25℃; for 1h; Inert atmosphere; | 88% |
With n-pentyl methyl ketone; Dimethylphenylsilane; triethylamine; (μ3;η2;η3;η5-acenaphthylene)Ru3(CO)7 In various solvent(s) at 20℃; for 2h; | 79% |
Conditions | Yield |
---|---|
With sulfuric acid In methanol at 5 - 35℃; for 2h; Solvent; Temperature; Large scale; | 95.61% |
Conditions | Yield |
---|---|
With sodium hydroxide In water; toluene for 72h; Autoclave; | 95% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol; water at 100℃; for 24h; | 91% |
Conditions | Yield |
---|---|
With formic acid at 190℃; for 6h; | 87% |
Conditions | Yield |
---|---|
With formic acid In methanol; water Reflux; | 75% |
Conditions | Yield |
---|---|
With (acetylacetonato)dicarbonylrhodium (l); dodecacarbonyl-triangulo-triruthenium; carbon monoxide; hydrogen; triphenylphosphine In N,N-dimethyl-formamide at 150℃; under 30003 Torr; for 1h; Autoclave; | 74% |
Conditions | Yield |
---|---|
With C19H32Cl2IrN2; potassium carbonate In water at 130℃; for 40h; Sealed tube; Green chemistry; | 70% |
Conditions | Yield |
---|---|
With (acetylacetonato)dicarbonylrhodium (l); dodecacarbonyl-triangulo-triruthenium; carbon monoxide; hydrogen; triphenylphosphine In N,N-dimethyl-formamide at 150℃; under 9000.9 Torr; for 1h; Autoclave; | A 8% B 69% |
non-1-ene
carbon monoxide
N,N-dimethyl-formamide
A
caprinaldehyde
B
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
With (acetylacetonato)dicarbonylrhodium (l); hydrogen; triphenylphosphine at 80℃; under 15001.5 Torr; for 3h; Autoclave; | A 65% B 7% |
Conditions | Yield |
---|---|
In methanol; water Reflux; | 63% |
non-1-ene
carbon monoxide
dimethyl amine
A
caprinaldehyde
B
N,N-dimethyldecylamine
C
decene-1-yl-dimethylamine
Conditions | Yield |
---|---|
With (acetylacetonato)dicarbonylrhodium (l); hydrogen; triphenylphosphine In N,N-dimethyl-formamide at 130℃; under 15001.5 Torr; for 3h; Autoclave; | A 9% B 45% C 16% |
With (acetylacetonato)dicarbonylrhodium (l); hydrogen; triphenylphosphine In N,N-dimethyl-formamide at 130℃; under 15001.5 Torr; for 1h; Autoclave; | A 13% B 44% C 10% |
With (acetylacetonato)dicarbonylrhodium (l); dodecacarbonyl-triangulo-triruthenium; hydrogen; triphenylphosphine In N,N-dimethyl-formamide at 80℃; under 9000.9 Torr; for 3h; Autoclave; | A 29% B 7% C 38% |
With (acetylacetonato)dicarbonylrhodium (l); dodecacarbonyl-triangulo-triruthenium; hydrogen; triphenylphosphine In N,N-dimethyl-formamide at 80℃; under 9000.9 Torr; for 6h; Autoclave; | A 21% B 21% C 29% |
non-1-ene
dimethyl amine
A
nonane
B
N,N-dimethyldecylamine
C
decene-1-yl-dimethylamine
Conditions | Yield |
---|---|
With (acetylacetonato)dicarbonylrhodium (l); carbon monoxide; hydrogen; triphenylphosphine In N,N-dimethyl-formamide at 150℃; under 9000.9 Torr; for 2h; Autoclave; | A 11% B 42% C 6% |
non-1-ene
carbon monoxide
N,N-dimethyl-formamide
A
caprinaldehyde
B
N,N-dimethyldecylamine
C
decene-1-yl-dimethylamine
Conditions | Yield |
---|---|
With (acetylacetonato)dicarbonylrhodium (l); hydrogen; triphenylphosphine at 130℃; under 15001.5 Torr; for 3h; Autoclave; | A 39% B 16% C 10% |
With (acetylacetonato)dicarbonylrhodium (l); hydrogen; triphenylphosphine at 150℃; under 30003 Torr; for 6h; Autoclave; | A 6% B 29% C 6% |
non-1-ene
carbon monoxide
dimethyl amine
A
caprinaldehyde
B
nonane
C
N,N-dimethyldecylamine
D
decene-1-yl-dimethylamine
Conditions | Yield |
---|---|
With (acetylacetonato)dicarbonylrhodium (l); hydrogen; triphenylphosphine In N,N-dimethyl-formamide at 150℃; under 9000.9 Torr; for 0.5h; Autoclave; | A 15% B 11% C 16% D 17% |
N,N-dimethyl-10-amino-1-decene
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
With ethyl acetate; platinum Hydrogenation; |
decyl-trimethyl-ammonium; hydroxide
A
1-Decanol
B
1-Decene
C
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
With sodium dimethylaminoborohydride In tetrahydrofuran at 66℃; for 55h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; | |
With ethanol; sodium In hexane at 0℃; for 0.333333h; Inert atmosphere; Overall yield = 73 %; Overall yield = 57.8 mg; chemoselective reaction; |
anhydro
A
6,7-dibenzoyl-1,3,5-triphenyl-cyclopenta[c]pyran
B
N,N-dimethyldecylamine
C
1,2,3-tribenzoylcyclopropane
D
1,4-diphenylbut-2-ene-1,4-dione
Conditions | Yield |
---|---|
at 150℃; for 3h; | A 400 mg B 2.85 g C n/a D 200 mg |
Conditions | Yield |
---|---|
In water at 140 - 150℃; |
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
With PS-triphenylphosphine; di-isopropyl azodicarboxylate In tetrahydrofuran |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: zinc chloride, hydrogen chloride / 140 °C 2: H2O / 140 - 150 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: benzene / 1.) 0 deg C, 1 h, 2.) r.t., 1 h 2: LiAlH4 / tetrahydrofuran / 5 h / Heating View Scheme |
1-Decanol
methylamine
A
N,N-dimethyldecylamine
B
N-methyldidecylamine
C
tri(n-decyl)amine
Conditions | Yield |
---|---|
filim type catalyst C at 185℃; for 4.5h; Product distribution / selectivity; | A 0.7 %Chromat. B 93.6 %Chromat. C 1.2 %Chromat. |
N,N-dimethyldecanamide
A
1-Decanol
B
N-decyl-N-methylamine
C
N,N-dimethyldecylamine
D
N-methyldidecylamine
Conditions | Yield |
---|---|
With hydrogen; dimethyl amine; CuCr catalyst (Leuna 1970T) at 250℃; under 7500.75 Torr; Product distribution / selectivity; | |
With hydrogen; dimethyl amine; CuCr catalyst Leuna 1970T at 250℃; under 7500.75 Torr; Product distribution / selectivity; Gas phase; | A 0.1 %Chromat. B 2.7 %Chromat. C 96.3 %Chromat. D 0.7 %Chromat. |
With hydrogen; CuCr catalyst (Leuna 1970T) at 250℃; under 7500.75 Torr; Product distribution / selectivity; | |
With hydrogen; CuCr catalyst Leuna 1970T at 250℃; under 7500.75 Torr; Product distribution / selectivity; Gas phase; | A 2.0 %Chromat. B 0.4 %Chromat. C 92.5 %Chromat. D 4.7 %Chromat. |
N,N-dimethyldecanamide
A
1-Decanol
B
N,N-dimethyldecylamine
C
N-methyldidecylamine
Conditions | Yield |
---|---|
With hydrogen; CuCr-type catalyst (Leuna 1970T) at 250℃; under 7500.75 Torr; Product distribution / selectivity; Gas phase; |
N,N-dimethyldecanamide
A
N-decyl-N-methylamine
B
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
With hydrogen; dimethyl amine; CuCr-type catalyst (Leuna 1970T) at 250℃; under 7500.75 Torr; Product distribution / selectivity; Gas phase; |
non-1-ene
Methyl formate
dimethyl amine
A
N,N-dimethyldecylamine
C
C12H27N
D
C12H27N
E
C12H27N
Conditions | Yield |
---|---|
With acetylacetonatodicarbonylrhodium(l); dodecacarbonyl-triangulo-triruthenium; water; triphenylphosphine In N,N-dimethyl-formamide at 170℃; for 6h; Autoclave; Green chemistry; |
Conditions | Yield |
---|---|
In acetone | 100% |
Conditions | Yield |
---|---|
In acetone | 100% |
Conditions | Yield |
---|---|
In acetonitrile at 82℃; for 48h; Menshutkin Reaction; | 99% |
In acetonitrile at 60℃; for 24h; | 92% |
Conditions | Yield |
---|---|
In acetonitrile at 40℃; for 239h; | 99% |
Conditions | Yield |
---|---|
In acetonitrile at 60℃; for 49h; | 99% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; benzonitrile; Mg-Al-O-t-Bu HT (Catalyst B) In methanol; water at 65℃; for 0.5h; Product distribution / selectivity; | 98% |
With dihydrogen peroxide; layered double hydroxide WO4(2-) at 20℃; for 2.5h; | 97% |
With dihydrogen peroxide In methanol; water | 75% |
With 1-decyl-4-(trifluoromethyl)pyrimidinium triflate; dihydrogen peroxide In aq. phosphate buffer; chloroform at 25℃; for 24h; Green chemistry; chemoselective reaction; | 67% |
Conditions | Yield |
---|---|
In acetonitrile at 82℃; for 48h; Menshutkin Reaction; | 97% |
In acetonitrile for 24h; Menshutkin Reaction; Heating; | 95% |
In acetonitrile at 60℃; for 24h; | 91% |
In methanol | 66% |
(1R,2S,5R)-1-(chloromethoxy)-2-isopropyl-5-methylcyclohexane
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
In hexane at 20℃; for 0.5h; Menschutkin reaction; | 97% |
Conditions | Yield |
---|---|
In acetonitrile at 82℃; for 48h; Menshutkin Reaction; | 97% |
In acetonitrile at 60℃; for 24h; | 93% |
In ethanol at 100℃; for 48h; |
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
In hexane at 20℃; for 3h; Menshutkin Reaction; | 96.5% |
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In ethanol for 8h; Reflux; | 95.8% |
Conditions | Yield |
---|---|
In acetonitrile at 60℃; for 24h; | 95% |
In methanol | 92% |
1-bromo dodecane
N,N-dimethyldecylamine
didecyldimethylammonium chloride
Conditions | Yield |
---|---|
Stage #1: 1-bromo dodecane; N,N-dimethyldecylamine Stage #2: With hydrogenchloride In water | 95% |
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
In acetonitrile for 2h; Reflux; | 95% |
Conditions | Yield |
---|---|
In acetonitrile for 24h; Menshutkin Reaction; Heating; | 94% |
Conditions | Yield |
---|---|
In methanol at 60℃; for 3h; Large scale; | 93.2% |
N,N-dimethyldecylamine
chloroacetonitrile
ethyl ester of p-toluenesulfonic acid
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyldecylamine; chloroacetonitrile In acetic acid butyl ester at 60℃; for 6h; Stage #2: ethyl ester of p-toluenesulfonic acid In acetic acid butyl ester at 80℃; for 1.5h; | 93% |
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
In acetonitrile for 2h; Reflux; | 93% |
N,N-dimethyldecylamine
Na(1+)*Ga(N3)4(1-)=Na[Ga(N3)4]
((CH3)2N(C10H21))Ga(N3)3
Conditions | Yield |
---|---|
In toluene Ar atmosphere, addn. of amine to solution of gallium compound at -78°C, warming to room temp. with stirring (12 h); filtration, removement of solvent (vacuum distillation, 25°C), washing (n-pentane); elem. anal.; | 92% |
Conditions | Yield |
---|---|
In acetonitrile for 24h; Menshutkin Reaction; Heating; | 92% |
With sodium carbonate In isopropyl alcohol at 55 - 83℃; for 8h; |
1-(bromomethyl)-4-(prop-1-en-2-yl)cyclohexene
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
In benzene at 20℃; Reflux; | 92% |
methyl 3α-bromoacetoxy-5β-cholan-24-oate
N,N-dimethyldecylamine
Conditions | Yield |
---|---|
In acetonitrile at 81℃; for 3h; | 91% |
N,N-dimethyldecylamine
3-Bromomethyl-1,8-dihydroxy-6-methoxy-9,10-anthraquinone
N-((4,5-dihydroxy-7-methoxy-9,10-anthraquinone-2-yl)methyl)-N,N-dimethyldecan-1-aminium bromide
Conditions | Yield |
---|---|
In chloroform for 24h; Reflux; | 90.1% |
1,4-bis(bromomethyl)benzene
N,N-dimethyldecylamine
1,4-bis[N-(1-decyl)-N,N-dimethylammoniummethyl]benzene dibromide
Conditions | Yield |
---|---|
In propan-1-ol for 8h; | 90% |
In methanol | 89% |
Conditions | Yield |
---|---|
In methanol at 120℃; for 48h; Autoclave; | 90% |
In methanol; ethylene glycol |
N,N-dimethyldecylamine
1,10-dibromodecane
N,N'-bis-decyl-N,N,N',N'-tetramethyl-N,N'-decanediyl-di-ammonium; dibromide
Conditions | Yield |
---|---|
In acetonitrile at 60℃; for 24h; | 90% |
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