Index Name Specifications Appearance Most yellow transparent liquid Assay 95.0 to 103.0% Acidity Tes
Cas:134-62-3
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inquiryItems Standard Result Appearance Clear,Colorless or light yellow liquid,free of foreign matter and suspended solids Colorless liquid
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inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
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Cas:134-62-3
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inquiryName: N,N-Diethyl-3-methylbenzamide CAS no. : 134-62-3 Molecular formula: C12H17NO Molecular weight:191.2695 Product Quality 12 years of chemical raw materials Mature operation of the industry System stability Data storage Security withou
Cas:134-62-3
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inquiryProduct Name: N,N-Diethyl-m-toluamide CAS: 134-62-3 MF: C12H17NO MW: 191.27 EINECS: 205-149-7 Mol File: 134-62-3.mol N,N-Diethyl-m-toluamide Structure N,N-Diethyl-m-toluamide Chemical Properties Melting point -45 °C Boilin
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Min.Order:1 Kilogram
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Min.Order:1 Gram
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Cas:134-62-3
Min.Order:100 Metric Ton
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With sodium hydroxide In water at 45℃; for 0.05h; Temperature; Reagent/catalyst; | 97.5% |
With benzene | |
With triethylamine Heating; Microwave irradiation; | |
With triethylamine In dichloromethane at 0 - 20℃; | |
at 0 - 20℃; for 20h; Alkaline conditions; |
Conditions | Yield |
---|---|
With triethylamine at 20℃; for 0.333333h; | 97.5% |
With triethylamine at 20℃; for 0.333333h; | 97.5% |
Conditions | Yield |
---|---|
With Zn-MCM-22 catalyst at 100 - 280℃; under 15001.5 Torr; for 6h; Inert atmosphere; Large scale; | 96% |
Stage #1: m-Toluic acid With niobium pentachloride In dichloromethane Stage #2: diethylamine In dichloromethane at 45 - 50℃; for 2.5h; | 85% |
hydroxy-apatite at 280 - 320℃; Product distribution; other catalysts; var. reaction time and temp.; influence of mineral acids with different pKa values; |
Conditions | Yield |
---|---|
With hydrogenchloride; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In 1,4-dioxane at 120℃; for 22h; | 91% |
Conditions | Yield |
---|---|
Stage #1: diethylamine With ethylmagnesium bromide In tetrahydrofuran; diethyl ether at 30℃; for 1h; Stage #2: 3-Methylbenzonitrile With ethylmagnesium bromide In diethyl ether; dichloromethane at 30℃; for 1h; Stage #3: With hydrogenchloride In tetrahydrofuran; diethyl ether; dichloromethane at 22℃; | 90% |
Conditions | Yield |
---|---|
With heptamethyl Coβ-perchlorato-cob(II)yrinate; tetrabutylammonium perchlorate In acetonitrile at 20℃; for 3h; Electrolysis; | 90% |
carbon monoxide
3-Iodotoluene
diethylamine
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
With palladium diacetate; triethylamine; triphenylphosphine In toluene at 80℃; for 18h; Sealed tube; | 89% |
With potassium carbonate In N,N-dimethyl-formamide at 120℃; under 750.075 Torr; for 2h; Autoclave; chemoselective reaction; | 85% |
With triethylamine In N,N-dimethyl acetamide at 130℃; under 15001.5 Torr; for 1.5h; Autoclave; Green chemistry; | 84% |
Conditions | Yield |
---|---|
With trifuran-2-yl-phosphane; palladium diacetate; 2,2-dimethylpropanoic anhydride In toluene at 120℃; for 15h; Inert atmosphere; | 89% |
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
at 200℃; for 0.0277778h; Product distribution / selectivity; microwave irradiation; | 88% |
2-(diethylamino)-2-oxoacetic acid
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; palladium diacetate In water; dimethyl sulfoxide; acetonitrile at 20℃; | 86% |
A
N,N-Diethyl-3-methylbenzamide
B
N-ethyl-m-Toluamide
Conditions | Yield |
---|---|
With tetrabutoxytitanium at 200℃; under 15001.5 Torr; for 0.0333333h; Product distribution / selectivity; microwave irradiation; | A 81% B 9% |
furfural
3-Iodotoluene
triethylamine
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
With Wilkinson’s catalyst; 1,3-bis-(diphenylphosphino)propane; water In tetrahydrofuran at 140℃; for 12h; Inert atmosphere; Sealed tube; | 80% |
Conditions | Yield |
---|---|
With silica gel; triethylamine; p-toluenesulfonyl chloride at 20℃; for 0.0166667h; | 76% |
With triethylamine at 20℃; for 0.0166667h; | 60% |
1,2:3,4-di-O-isopropylidene-α-D-galactopyranose
N,N-diethyl-α,α-difluoro-(meta-methylbenzyl)amine
A
6-deoxy-6-fluoro-1,2:3,4-di-O-isopropylidene-α-D-galctopyranose
B
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
In n-heptane for 0.333333h; microwave irradiation; | A 70% B n/a |
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); sodium t-butanolate In toluene at 20 - 180℃; for 14h; Inert atmosphere; Glovebox; Sealed tube; | 64% |
N,N-Diethyl-3-methyl-2-(2-methyl-propane-2-sulfonyl)-benzamide
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol for 15h; Heating; | 55% |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: H2O2 / acetic acid / 3 h / 100 °C 2: 1.) n-BuLi / 1.) THF, -78 deg C, 0.5 h, 2.) -78 deg C 3: 1.) n-BuLi / 1.) THF, -78 deg C, 30 min, 2.) -78 deg C 4: 55 percent / H2 / Raney Ni / ethanol / 15 h / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.) n-BuLi / 1.) THF, -78 deg C, 0.5 h, 2.) -78 deg C 2: 1.) n-BuLi / 1.) THF, -78 deg C, 30 min, 2.) -78 deg C 3: 55 percent / H2 / Raney Ni / ethanol / 15 h / Heating View Scheme |
2-<(1,1-dimethylethyl)sulphonyl>-N,N'-diethylbenzamide
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) n-BuLi / 1.) THF, -78 deg C, 30 min, 2.) -78 deg C 2: 55 percent / H2 / Raney Ni / ethanol / 15 h / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: tetrahydrofuran / -78 °C 2: H2O2 / acetic acid / 3 h / 100 °C 3: 1.) n-BuLi / 1.) THF, -78 deg C, 0.5 h, 2.) -78 deg C 4: 1.) n-BuLi / 1.) THF, -78 deg C, 30 min, 2.) -78 deg C 5: 55 percent / H2 / Raney Ni / ethanol / 15 h / Heating View Scheme |
Conditions | Yield |
---|---|
sodium ethanolate at 305℃; under 26252.6 Torr; for 0.00944444h; autoclave; Industry scale; Microwave irradiation; |
ortho-methylbenzoic acid
thionyl chloride
dichloromethane
dibenzylamine
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
Stage #1: ortho-methylbenzoic acid; thionyl chloride; dichloromethane With N,N-dimethyl-formamide for 2h; Reflux; Stage #2: dibenzylamine at 20℃; |
Conditions | Yield |
---|---|
In ethyl acetate at 50℃; Sealed tube; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium hydrogencarbonate; iron(III) chloride; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / acetonitrile; water / 35 °C 2: ethyl acetate / 50 °C / Sealed tube View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1,3,5-trichloro-2,4,6-triazine; 1-pyrrolidinecarboxaldehyde / acetonitrile / Heating 2: 20 h / 0 - 20 °C / Alkaline conditions View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 2 h / 0 - 20 °C 1.2: 0 - 20 °C 2.1: zinc(II) chloride; diisobutylaluminium hydride; magnesium; lithium chloride / tetrahydrofuran / 6 h / 20 °C / Inert atmosphere 2.2: 50 °C / Inert atmosphere 3.1: bis(1,5-cyclooctadiene)nickel (0); sodium t-butanolate / toluene / 14 h / 20 - 180 °C / Inert atmosphere; Glovebox; Sealed tube View Scheme |
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: zinc(II) chloride; diisobutylaluminium hydride; magnesium; lithium chloride / tetrahydrofuran / 6 h / 20 °C / Inert atmosphere 1.2: 50 °C / Inert atmosphere 2.1: bis(1,5-cyclooctadiene)nickel (0); sodium t-butanolate / toluene / 14 h / 20 - 180 °C / Inert atmosphere; Glovebox; Sealed tube View Scheme |
N,N-Diethyl-3-methylbenzamide
N-ethyl-N-(3-methylbenzyl)ethanamine
Conditions | Yield |
---|---|
With n-butyllithium; borane-THF; diisopropylamine at 25℃; | 99% |
With lithium (diisopropylamino)borohydride In tetrahydrofuran at 25℃; for 2h; | 99% |
With diisobutylaluminum borohydride In tetrahydrofuran at 0 - 25℃; Inert atmosphere; | 99% |
styrene
N,N-Diethyl-3-methylbenzamide
N,N-diethyl-5-methyl-2-(1-phenylethyl)benzamide
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)iridium(I) tetrakis[3,5-bis(trifluoromethyl)phenyl]borate; 1,4-bis[bis(pentafluorophenyl)phosphino]butane In 1,4-dioxane at 100℃; for 48h; Sealed tube; Inert atmosphere; | 99% |
N,N-Diethyl-3-methylbenzamide
N,N-diethyl-αlpha;-chloro-meta-toluylamidinum chloride
Conditions | Yield |
---|---|
With oxalyl dichloride In tetrachloromethane at 0 - 50℃; for 1.5h; | 98% |
With oxalyl dichloride In tetrachloromethane at 0 - 50℃; for 1.5h; | 98% |
With oxalyl dichloride In tetrachloromethane at 0 - 50℃; for 1.5h; | |
With oxalyl dichloride In tetrachloromethane at 0 - 50℃; for 1.5h; |
1,1,1,3,5,5,5-heptamethyltrisiloxan
N,N-Diethyl-3-methylbenzamide
C19H37NO3Si3
Conditions | Yield |
---|---|
With [Rh(coe)2OH]2; 3,4,5-MeO-MeO-BIPHEP; cyclohexene In tetrahydrofuran at 45℃; regioselective reaction; | 96% |
With (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 2.9-dimethyl-1,10-phenanthroline In 1,4-dioxane at 100℃; for 20h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; Sealed tube; regioselective reaction; | 63% |
Conditions | Yield |
---|---|
With pyrrolidine; n-butyllithium; borane-THF at 25℃; | 95% |
With LiPyrrBH3 In tetrahydrofuran at 25℃; for 2h; | 95% |
N,N-Diethyl-3-methylbenzamide
bis(pinacol)diborane
Conditions | Yield |
---|---|
With (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine In hexane at 80℃; for 18h; Inert atmosphere; Sealed tube; regioselective reaction; | 95% |
Stage #1: bis(pinacol)diborane With C24H28ClIrN2O In n-heptane; isopropyl alcohol at 75℃; for 1h; Sealed tube; Inert atmosphere; Stage #2: N,N-Diethyl-3-methylbenzamide In n-heptane; isopropyl alcohol Sealed tube; Inert atmosphere; | 87% |
Stage #1: bis(pinacol)diborane With (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2’-bipyridine In hexane at 60℃; for 0.5h; Inert atmosphere; Glovebox; Sealed tube; Stage #2: N,N-Diethyl-3-methylbenzamide With bis(2,6-di-tert-butyl-4-methylphenoxide)methylaluminum In hexane at 20℃; for 18h; Sealed tube; | 55% |
N,N-Diethyl-3-methylbenzamide
N,N-diethyl-3-methylthiobenzamide
Conditions | Yield |
---|---|
With triethylamine; trichlorophosphate In water at 60 - 70℃; for 0.0833333h; microwave irradiation; | 89% |
With trichlorothiophosphine; water; triethylamine Microwave irradiation; | 89% |
With trichlorothiophosphine; water; triethylamine Heating; Microwave irradiation; |
N,N-Diethyl-3-methylbenzamide
(4-(dimethylamino)phenyl)(m-tolyl)methanone
Conditions | Yield |
---|---|
at 0℃; for 1h; Inert atmosphere; Schlenk technique; | 86% |
N,N-Diethyl-3-methylbenzamide
N,N-diethyl-α,α-difluoro-(meta-methylbenzyl)amine
Conditions | Yield |
---|---|
Stage #1: N,N-Diethyl-3-methylbenzamide With oxalyl dichloride In dichloromethane at 40℃; for 2h; Stage #2: With triethylamine tris(hydrogen fluoride); triethylamine In dichloromethane at 20℃; for 2h; | 82% |
Stage #1: N,N-Diethyl-3-methylbenzamide With oxalyl dichloride In dichloromethane at 40℃; for 2h; Stage #2: With triethylamine tris(hydrogen fluoride); triethylamine In dichloromethane at 20℃; for 2h; Further stages.; | 82% |
With Carbonyl fluoride In 1,2-dichloro-ethane at 158℃; for 10h; Product distribution / selectivity; | 60% |
With Carbonyl fluoride at 72 - 170℃; for 10h; Product distribution / selectivity; | 7% |
N,N-Diethyl-3-methylbenzamide
Conditions | Yield |
---|---|
With water In dichloromethane at 45℃; for 6h; | 82% |
With water at 60℃; for 18h; | 82% |
Conditions | Yield |
---|---|
With hydrogenchloride; iron(III) chloride hexahydrate In hexane; water at 80℃; for 14h; | 81% |
Conditions | Yield |
---|---|
With niobium(V) oxide; water In neat (no solvent) for 24h; Reflux; Inert atmosphere; | 76% |
2,3-dimethyl-2,3-butane diol
Trimethyl borate
N,N-Diethyl-3-methylbenzamide
pinacolo[2-(N,N-diethylcarboxamido)-4-methylphenyl]boronate
Conditions | Yield |
---|---|
With N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium In tetrahydrofuran (Ar); soln. of benzamide in THF was added dropwise to stirred soln. of s-BuLi/tetramethylethylenediamine (1/1) in THF at -78°C; mixt. wasstirred at -78°C for 1 h; treated with B(OMe)3; mixt. was warmed to room temp. over 8-12 h; quenched with satd. aq. NH4Cl; aq. phase extd. (Et2O); extract dried (Na2SO4); concd. (vac.); chromd. (silica gel, EtOAc/hexane); stirred with pinacol and MgSO4 in CH2Cl2 for 12 h; filtered; concd.; chromd. (silica gel, EtOAc/hexane, 1/3); | 70% |
N,N-Diethyl-3-methylbenzamide
A
3-methylbenzyl alcohol
B
m-tolyl aldehyde
Conditions | Yield |
---|---|
With titanium(IV) isopropylate; 1,1,3,3-Tetramethyldisiloxane In methyl cyclohexane at 20℃; for 15h; Inert atmosphere; | A Ca. 10 %Spectr. B 70% |
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; copper diacetate; lithium fluoride In 1,2-dichloro-ethane at 120℃; for 36h; Schlenk technique; | 68% |
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