Appearance Colorless to slightly yellow transparent liquid Color (Gardener) ≤ 2.0 Assay ≥99.0% Acid Value(mgKOH/g) ≤ 5
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inquiryN,N-Dimethylcapramide Basic information Product Name: N,N-Dimethylcapramide Synonyms: TIMTEC-BB SBB008016;N,N-DIMETHYLCAPRAMIDE;N,N-DIMETHYLDECANAMIDE;Decanamide, N
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N,N-Dimethyldecanamid Synonyms: N,N-Dimethylcapramide Cas No: 14433-76-2 Molecular Formula:C12H25NO Quality Index Item Index Appearance Clear liquid Purity
Cas:14433-76-2
Min.Order:1 Kilogram
Negotiable
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inquiryConditions | Yield |
---|---|
With C19H26ClIrNOP; potassium tert-butylate In toluene at 80℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; Green chemistry; | 94% |
With C29H55IrN3P2(1+)*Cl(1-); potassium tert-butylate In toluene at 120℃; for 15h; Schlenk technique; Inert atmosphere; Glovebox; | 76% |
With C20H37ClN2OPRu; potassium tert-butylate In neat liquid at 140℃; for 24h; Inert atmosphere; | 36% |
Conditions | Yield |
---|---|
In benzene at 20℃; | 93% |
In benzene 1.) 0 deg C, 1 h, 2.) r.t., 1 h; |
N,N-dimethylammonium chloride
n-decanoyl chloride
N,N-dimethyldecanamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 76% |
1-decanoic acid
N,N-dimethyl-formamide
N,N-dimethyldecanamide
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; copper(II) perchlorate hexahydrate at 100℃; for 6h; | 65% |
S-phenyl decanethioate
N,N-dimethyl-formamide
N,N-dimethyldecanamide
Conditions | Yield |
---|---|
With lithium perchlorate Electrochemical reaction; | 32 % Spectr. |
Conditions | Yield |
---|---|
Stage #1: 1-decanoic acid; dimethyl amine In water Stage #2: In water at 240℃; under 15001.5 Torr; for 0.166667h; Product distribution / selectivity; Microvawe irradiation; |
N,N-dimethyldecanamide
1-dimethylaminodecyl-1,1-bisphosphonic acid
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyldecanamide With phosphorous acid; phosphorus trichloride at 70℃; for 2h; Stage #2: With water for 2h; | 100% |
Stage #1: N,N-dimethyldecanamide With phosphorous acid; phosphorus trichloride at 70℃; for 12h; Stage #2: With water for 2h; | 100% |
Stage #1: N,N-dimethyldecanamide With phosphonic Acid; phosphorus trichloride at 70℃; for 2h; Stage #2: With water at 100℃; for 3h; | 100% |
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% |
N,N-dimethyldecanamide
Conditions | Yield |
---|---|
With water In toluene at 80℃; for 3h; | 85% |
With water at 60℃; for 18h; | 85% |
Conditions | Yield |
---|---|
With water at 60℃; for 20h; | 85% |
N,N-dimethyldecanamide
N,N-dimethyldecane-1-amine hydrochloride
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyldecanamide With bis(cyclopentadienyl)dihydrozirconium; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane at 20℃; under 760.051 Torr; for 12h; Inert atmosphere; Stage #2: With hydrogenchloride In diethyl ether Inert atmosphere; | 83% |
N,N-dimethyldecanamide
dimethyl(phenyl)silyllithium
decanoyldimethyl(phenyl)silane
Conditions | Yield |
---|---|
In tetrahydrofuran at -78℃; for 1.5h; | 82% |
N,N-dimethyldecanamide
lithium sodium dianion of methyl acetoacetate
methyl 3,5-dioxotetradecanoate
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In tetrahydrofuran; hexane at -78 - 0℃; for 2h; | 74% |
With boron trifluoride diethyl etherate; silica gel 1.)tetrahydrofuran, -78 --> 0 deg C, 2 h, 2.)room temp., overnight; Yield given. Multistep reaction; |
N,N-dimethyldecanamide
α-(dimethylamino)decyl cyanide
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyldecanamide With bis(triphenylphosphine)iridium(I) carbonyl chloride In toluene at 20℃; for 0.0833333h; Stage #2: With 1,1,3,3-Tetramethyldisiloxane In toluene at 20℃; for 0.0833333h; Stage #3: With trimethylsilyl cyanide In toluene at 20℃; for 0.5h; | 72% |
Conditions | Yield |
---|---|
With sodium t-butanolate In neat (no solvent) at 80℃; for 12h; Temperature; Inert atmosphere; Glovebox; | 72% |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyldecanamide With bis(triphenylphosphine)carbonyliridium(I) chloride; 1,1,3,3-Tetramethyldisiloxane In dichloromethane at 20℃; for 0.333333h; Stage #2: benzylmagnesium chloride at -78 - 20℃; for 4h; | 58% |
N,N-dimethyldecanamide
1-Decanol
Conditions | Yield |
---|---|
With ethanol; sodium In hexane; paraffin oil at 0℃; for 0.0833333h; Inert atmosphere; | 42% |
N,N-dimethyldecanamide
2-octyl-3-oxo-dodecanoic acid dimethylamide
Conditions | Yield |
---|---|
With trichlorophosphate; benzene |
Conditions | Yield |
---|---|
With trichlorophosphate; benzene |
Conditions | Yield |
---|---|
With sodium hydroxide; water; trichlorophosphate 1) benzene, 18 h, 20 deg C, 2) 1 h, 20 deg C; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
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; |
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
N,N-dimethyldecanamide
Conditions | Yield |
---|---|
With titanium(IV) isopropylate; diphenylsilane at 20℃; Yield given; |
Conditions | Yield |
---|---|
With n-butyllithium 1) THF, hexane, -78 deg C, 2) THF, hexane, -78 deg C, 30 min; Yield given. Multistep reaction; |
2,4-dithiapentane
N,N-dimethyldecanamide
1,1,1-Tris-methylsulfanyl-undecan-2-one
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
N,N-dimethyldecanamide
caprinaldehyde
Conditions | Yield |
---|---|
With bis-(1,2-dimethylpropyl)borane In tetrahydrofuran; dodecane at 25℃; | 85 % Chromat. |
Multi-step reaction with 2 steps 1: Ti(O-i-Pr)4, Ph2SiH2 / 20 °C 2: 1 M aq. HCl / tetrahydrofuran / 20 °C View Scheme | |
With C11H25AlNO4(1-)*Na(1+) In tetrahydrofuran; toluene at 0 - 20℃; for 0.5h; | > 99 %Chromat. |
With benzoic acid ethyl ester; copper diisobutyl-t-butoxyaluminum hydride In tetrahydrofuran at 20℃; for 12h; Reagent/catalyst; Inert atmosphere; chemoselective reaction; | > 99 %Chromat. |
N,N-dimethyldecanamide
Conditions | Yield |
---|---|
With dimethyl(phenyl)silyl lithium In tetrahydrofuran at -78 - -20℃; for 1h; | |
With dimethyl(phenyl)silyl lithium In tetrahydrofuran at -78 - -20℃; for 2h; |
N,N-dimethyldecanamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: PhMe2SiLi / tetrahydrofuran / 2 h / -78 - -20 °C 2: 243 mg / aq. HCl / 18 h / 70 °C View Scheme | |
Multi-step reaction with 2 steps 1: PhMe2SiLi / tetrahydrofuran / 1 h / -78 - -20 °C 2: H2O, HCl View Scheme |
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