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inquiryProduct Description Product website: http://www.finerchem.com Product Name 2,4,6-Trimethylbenzenamine CAS No. 88-05-1 Appearance
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inquiryUnique advantages for 2,4,6-Trimethylaniline Cas 88-05-1 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Light yellow liquid Storage:Store below +30°C Package:180kg/drum App
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inquiry2,4,6-Trimethylaniline Basic information Product Name: 2,4,6-Trimethylaniline Synonyms: 1-amino-2,4,6-trimethylbenzen;1-amino-2,4,6-trimethylbenzen(czech);1-Amino-2,4,6-trimethylbenzene;
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inquiryName: 2,4,6-Trimethylaniline CAS NO.: 88-05-1 Molecular formula: C9H13N Appearance:light yellow oily liquid Storage:Preserve in well-closed, light-resistant and airtight containers. Package:25kg Application:d
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inquiryProduct Name: 2,4,6-Trimethylaniline CAS: 88-05-1 MF: C9H13N MW: 135.21 EINECS: 201-794-3 Mol File: 88-05-1.mol 2,4,6-Trimethylaniline Structure 2,4,6-Trimethylaniline Chemical Properties Melting point -5 °C Boiling point
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inquirysuperior quality Appearance:clear yellow to brown liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Mainly used in synthetic dyes, is a weak
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inquiry1-Benzyl-1,4-dihydronicotinamide
A
1-benzyl-3-carbamoylpyridinium ion
B
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
In acetonitrile at 25℃; Kinetics; | A 100% B 85% |
N-methyl-2,4,6-trimethylaniline
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With dichloro(dimethylglyoxime)(dimethylglyoximato)cobalt(III); (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; triethylamine In acetonitrile at -78℃; for 24h; Reagent/catalyst; Sealed tube; Inert atmosphere; Irradiation; | 100% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In tetrahydrofuran for 12h; | 99% |
With titanium tetrachloride; di-isobutyl telluride In dichloromethane for 0.5h; Ambient temperature; | 98% |
With hydrogen In tetrahydrofuran; water at 120℃; under 37503.8 Torr; for 24h; chemoselective reaction; | 96% |
Conditions | Yield |
---|---|
With 2-((dicyclohexylphosphino)methyl)-1,3-bis(2,6-diisopropylphenyl)-4,5-dimethyl-1H-imidazol-3-ium iodide; ammonia; palladium diacetate; sodium t-butanolate In 1,4-dioxane at 120℃; under 7500.75 Torr; for 24h; Autoclave; Inert atmosphere; | 99% |
With copper(l) iodide; sodium azide; N,N`-dimethylethylenediamine In dimethyl sulfoxide at 100℃; for 10h; Inert atmosphere; | 72% |
Stage #1: 2,4,6-trimethylphenyl bromide With magnesium In tetrahydrofuran Inert atmosphere; Stage #2: With 3-tert-butyl-3-phenyloxaziridine In tetrahydrofuran; toluene at -45℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water; toluene Reagent/catalyst; Inert atmosphere; | 31% |
Conditions | Yield |
---|---|
With methanol; O-benzenesulfonyl-acetohydroxamic acid ethyl ester; toluene-4-sulfonic acid at 23℃; for 24h; Inert atmosphere; | 96% |
With ethanol; hydroxylamine hydrochloride at 160℃; und Erhitzen mit Salzsaeure im Druckrohr; |
anti-2,2',4,4',6,6'-Hexamethylazobenzene
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With sodium dithionite In methanol; dichloromethane; water for 3h; Heating; | 96% |
Conditions | Yield |
---|---|
With disodium telluride In 1,4-dioxane; water at 50℃; for 2h; | A 95% B n/a |
N,N-dibenzyl-2,4,6-trimethylaniline
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With formic acid; potassium hydroxide In ethanol at 70℃; for 1h; | 95% |
carbon monoxide
nitromesitylene
A
mesityl isocyanate
B
1,3-bis(2,4,6-trimethylphenyl)urea
C
anti-2,2',4,4',6,6'-Hexamethylazobenzene
D
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
Vanadium (III) chloride-(tris-tetrahydrofuran); (Bu4N) In various solvent(s) at 120℃; for 0.5h; Product distribution; further catalysts, other reaction times; | A 94% B n/a C n/a D n/a |
Vanadium (III) chloride-(tris-tetrahydrofuran); (Bu4N) In various solvent(s) at 120℃; for 0.5h; | A 94% B n/a C n/a D n/a |
2,3,5,6-tetrafluoro-4-(2,4,6-trimethylphenylazo)pyridine
A
2,3,5,6-tetrafluoropyridin-4-amine
B
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With sodium disulfite; hydrogen iodide for 1h; Heating; | A 31% B 93% |
Conditions | Yield |
---|---|
In acetonitrile at 25℃; Kinetics; | A 93% B 78% |
Conditions | Yield |
---|---|
With copper(I) oxide; ammonium hydroxide; air In methanol at 20℃; for 12h; | 92% |
With caesium carbonate; O-(2,4-dinitrophenyl)hydroxylamine In 1,2-dichloro-ethane at 25℃; for 48h; Inert atmosphere; | 42% |
Conditions | Yield |
---|---|
With tert-butyl N-tosyloxycarbamate at 20℃; for 36h; Solvent; Reagent/catalyst; Temperature; Concentration; chemoselective reaction; | 89% |
With 16-crown-6; 1-aminoquinolinium perchlorate In trifluoroacetic acid for 4h; Irradiation; | 80% |
With hydrogenchloride; aluminium trichloride; sodium azide In various solvent(s) at 20℃; | 76% |
N-(diphenyl methylene)-2,4,6-trimethylaniline
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
Acid hydrolysis; | 87% |
2,4,6-trimethylphenyl p-toluenesulfonate
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With bis(tri-ortho-tolylphosphine)palladium(0); (R)-(-)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl-di-tert-butylphosphine; ammonia; sodium t-butanolate In 1,4-dioxane at 50℃; for 24h; Inert atmosphere; | 86% |
(2,4,6-trimethyl-phenyl)-carbamic acid tert-butyl ester
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With methanol; oxalyl dichloride at 20℃; for 2h; | 83% |
1-fluoro-2,4,6-trimethylbenzene
potassium enolate of acetone
A
1-(2,4,6-trimethylphenyl)-2-propanone
B
1-(2,4,6-Trimethylphenyl)-2-propanol
C
2,4,6-trimethylaniline
D
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With ammonia; potassium amide at -33℃; Product distribution; Rate constant; | A 2.8% B 5.6% C 11.7% D 80% |
With ammonia; potassium amide at -33℃; | A 1.8 % Chromat. B 3.1 % Chromat. C 18.2 % Chromat. D 77 % Chromat. |
With ammonia; potassium amide at -33℃; | A 2.8 % Chromat. B 5.6 % Chromat. C 11.7 % Chromat. D 80 % Chromat. |
dimesityl-1,3-tetraphenylcyclodigermazane
3,5-di-tert-butyl-o-benzoquinone
A
2,2-diphenyl(6,8-di-t-butyl)-4,5-benzo-2-germa-1,3-dioxolane
B
ditertiobutyl-2,4 (trimethyl-2,4,6 phenylimino)-6 cyclohexadiene-2,4 one-1
C
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
In benzene-d6 inert atmosphere (Ar or N2); 100°C, 12 h; not isolated; (1)H-NMR; | A n/a B <1 C 80% |
(C6H5)2ClGeNHC6H2(CH3)3
3,5-di-tert-butyl-o-benzoquinone
A
2,2-diphenyl(6,8-di-t-butyl)-4,5-benzo-2-germa-1,3-dioxolane
B
ditertiobutyl-2,4 (trimethyl-2,4,6 phenylimino)-6 cyclohexadiene-2,4 one-1
C
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In benzene-d6 byproducts: DBU*HCl; inert atmosphere (Ar or N2); 20°C, 17 h; (1)H-NMR; evapn., pentane addn., filtn.; | A 67% B <1 C 80% |
Conditions | Yield |
---|---|
With ammonium sulfate; bis(1,5-cyclooctadiene)nickel (0); sodium t-butanolate at 100 - 110℃; for 12h; | 72% |
Conditions | Yield |
---|---|
Stage #1: mesitylenecarboxylic acid With trifluorormethanesulfonic acid; trimethylsilylazide In chloroform at 90℃; for 0.06h; Schmidt Reaction; Flow reactor; Stage #2: With water In methanol; chloroform at 20℃; Schmidt Reaction; Flow reactor; | 71% |
2,4,6-trimethylphenyl bromide
A
2,4,6-trimethylaniline
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With sodium amide In diethyl ether; ammonia for 2h; Irradiation; | A 70% B 6% |
With sodium amide In diethyl ether; ammonia for 2h; Product distribution; Irradiation; variation of reaction conditions; | A 70% B 6% |
N-(tert-butoxycarbonyl)-O-(mesitylsulfonyl)hydroxylamine
1,3,5-trimethyl-benzene
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}; trifluoroacetic acid In 2,2,2-trifluoroethanol at 0℃; for 25h; regioselective reaction; | 70% |
With Rh2(esp)2; trifluoroacetic acid In 2,2,2-trifluoroethanol at 0 - 20℃; for 25h; Inert atmosphere; | 70% |
18-crown-6 ether
B
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
In benzene at 20℃; for 12h; Inert atmosphere; | A 70% B n/a |
Conditions | Yield |
---|---|
With ammonium hydroxide; potassium phosphate; 1-(5,6,7,8-tetrahydroquinolin-8-yl)-2-methylpropan-1-one; copper(I) bromide In dimethyl sulfoxide at 80℃; for 24h; Inert atmosphere; Sealed tube; | 60% |
Conditions | Yield |
---|---|
In acetonitrile at 25℃; Kinetics; | A 26% B 60% |
2,4-di-tert-Butylphenol
A
3,3',5,5'-tetra(tert-butyl)biphenyl-2,2'-diol
C
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
In acetonitrile at 20℃; Inert atmosphere; | A 25% B n/a C 56% |
N,N'-bis(2,4,6-trimethylphenyl)ethanediimine
1,2-phenylenediacetonitrile
A
naphthalene-1,4-dicarbonitrile
B
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With potassium hydroxide In N,N-dimethyl-formamide at 100℃; for 15h; | A 54% B n/a |
azidotri-2,4,6-trimethylphenylgermane
A
diethoxybis(2,4,6-trimethylphenyl)germane
B
Ge(C6H2(CH3)3)2NHCH2(C6H2(CH3)2)
C
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With ethanol In ethanol; cyclohexane | A 14% B 50% C 11% |
mesitylenesulfonylhydroxylamine
1,3,5-trimethyl-benzene
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}; trifluoroacetic acid In 2,2,2-trifluoroethanol at 0℃; for 0.5h; regioselective reaction; | 49% |
With Rh2(esp)2 In 2,2,2-trifluoroethanol at 0℃; for 0.5h; Inert atmosphere; | 49% |
phthalic anhydride
2,4,6-trimethylaniline
1-(N-phthalimido)-2,4,6-trimethylbenzene
Conditions | Yield |
---|---|
With acetic acid at 150℃; for 2h; Inert atmosphere; | 100% |
With acetic acid at 140℃; for 12h; | 90% |
With 1H-imidazole at 140℃; for 3h; Inert atmosphere; Schlenk technique; | 22% |
Conditions | Yield |
---|---|
at 0 - 20℃; for 2.5h; Inert atmosphere; Schlenk technique; | 100% |
With sulfonic acid-functionalized hyper-cross-linked poly(2-naphthol) In neat (no solvent) at 25℃; for 0.166667h; Green chemistry; chemoselective reaction; | 93% |
With N,N,N-trimethyl-2-(sulfooxy)ethanaminium chloride In neat (no solvent) at 20℃; for 0.216667h; Milling; Green chemistry; | 90% |
Ethyl oxalyl chloride
2,4,6-trimethylaniline
2-(2,4,6-trimethylphenylamino)-2-oxoacetic acid ethyl ester
Conditions | Yield |
---|---|
With pyridine at 20℃; for 1.5h; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 97% |
In tetrahydrofuran at 70℃; for 1h; | 96% |
p-Toluic acid
2,4,6-trimethylaniline
N-(2,4,6-trimethylphenyl)-4-methylbenzamide
Conditions | Yield |
---|---|
With diphosphorus tetraiodide In tetrachloromethane; dichloromethane Heating; | 100% |
Conditions | Yield |
---|---|
With copper(II) dipivaloate In dichloromethane for 0.0833333h; Product distribution; Ambient temperature; other BiV reagents; copper-catalyzed phenylation of amines by BiV reagents; | 100% |
copper In dichloromethane for 24h; Ambient temperature; | 92% |
With copper(II) dipivaloate In dichloromethane for 0.0833333h; Ambient temperature; | 100 % Chromat. |
di-tert-butyl dicarbonate
2,4,6-trimethylaniline
(2,4,6-trimethyl-phenyl)-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With indium(III) bromide at 30 - 35℃; for 0.5h; | 100% |
Stage #1: 2,4,6-trimethylaniline With triethylamine In tetrahydrofuran; water at 20℃; for 0.0833333h; Stage #2: di-tert-butyl dicarbonate In tetrahydrofuran; water at 0 - 20℃; for 6h; | 100% |
In tetrahydrofuran for 168h; Heating; | 98% |
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
Stage #1: trifluoromethyl dihydro-1,4-dioxin-3-carbonyl chloride With pyridine; polystyrene-bound 4-hydroxy-3-nitrobenzophenone In dichloromethane at 20℃; for 24h; Acylation; Stage #2: 2,4,6-trimethylaniline With triethylamine In acetonitrile for 14h; Acylation; Heating; | 100% |
phenylacetylene
2,4,6-trimethylaniline
N-(1-phenylethylidene)-2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With [Zn2Cp*3]+[B(3,5-(CF3)2C6H3)4]- at 20℃; for 72h; Reagent/catalyst; Inert atmosphere; Schlenk technique; regioselective reaction; | 100% |
With C18H5AlF36O4Zn In benzene-d6 at 60℃; for 1h; Inert atmosphere; regioselective reaction; | 100% |
With C30H36FeP2*2Au(1+)*Cl(1-)*C32H12BF24(1-) In (2)H8-toluene at 120℃; for 6h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Sealed tube; Glovebox; | 100% |
2,4,6-trimethylaniline
(Z)-4-[2,4,6-Tris-(bis-trimethylsilanyl-methyl)-phenylamino]-pent-3-en-2-one
C41H78N2Si6
Conditions | Yield |
---|---|
With titanium tetrachloride In toluene for 16h; Heating; | 100% |
With titanium tetrachloride In toluene for 16h; Heating; | 94% |
2,4,6-trimethylaniline
1,2-dibromobenzene
N1,N2-bis(2,4,6-trimethylphenyl)-1,2-benzenediamine
Conditions | Yield |
---|---|
With ammonium chloride; sodium t-butanolate; palladium diacetate In water; argon; toluene | 100% |
With tri-tert-butylphosphonium tetrafluoroborate; palladium diacetate; sodium t-butanolate In toluene at 60 - 135℃; Inert atmosphere; | 87% |
With 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; palladium diacetate In toluene for 12h; Heating; | 86% |
Conditions | Yield |
---|---|
With hydrogenchloride In diethyl ether at 0 - 20℃; for 0.5h; | 100% |
3-nitrophenyl isothiocyanate
2,4,6-trimethylaniline
1-(mesityl)-3-(3-nitrophenyl)thiourea
Conditions | Yield |
---|---|
In methanol at 20℃; for 2h; | 100% |
In methanol at 20℃; for 2h; |
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
acetic acid In ethanol at 20℃; | 100% |
2-bromoisobutyric acid bromide
2,4,6-trimethylaniline
2-bromo-N-mesityl-2-methylpropanamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; for 3h; Inert atmosphere; | 94% |
orthoformic acid triethyl ester
2,4,6-trimethylaniline
N,N'-dimesitylformamidine
Conditions | Yield |
---|---|
With acetic acid In neat (no solvent) at 160℃; for 3h; | 100% |
With acetic acid In neat (no solvent) at 120 - 160℃; for 4h; | 98% |
With acetic acid at 90 - 120℃; for 4 - 6h; Product distribution / selectivity; | 92% |
Conditions | Yield |
---|---|
With C18H5AlF36O4Zn In benzene-d6 at 60℃; for 8h; Inert atmosphere; regioselective reaction; | 100% |
With AuC34H47N(1+)*B(C6F5)4(1-)=(AuC34H47N)(B(C6F5)4) In benzyl methyl ether; benzene-d6 at 90℃; for 24h; Inert atmosphere; | 82 %Spectr. |
(C4HN(adamantyl)Me2(2,6-diisopropylphenyl))AuCl; potassium tetrakis(pentafluorophenyl)borate In benzyl methyl ether; benzene-d6 at 90℃; for 24h; Product distribution / selectivity; Inert atmosphere; | 82 %Spectr. |
2,4,6-trimethylaniline
4-n-methylphenylacetylene
2,4,6-trimethyl-N-(1-(p-tolyl)ethylidene)aniline
Conditions | Yield |
---|---|
With C18H5AlF36O4Zn In benzene-d6 at 60℃; for 1h; Inert atmosphere; regioselective reaction; | 100% |
With silver tetrafluoroborate; {(2,6-bis(1-isopropyl-2,3-dihydro-1H-imidazole-2-thione)pyridine)12Cu8}(PF6)8 In acetonitrile at 70℃; Reagent/catalyst; Schlenk technique; Inert atmosphere; regioselective reaction; | 98% |
With silver tetrafluoroborate; [1-(3,3-dimethyl-2-oxobutyl)-4-benzyl-1,2,4-triazol-5-ylidene]AuCl; acetonitrile at 90℃; for 12h; regioselective reaction; | 93 %Chromat. |
4-bromo-1-ethynylbenzene
2,4,6-trimethylaniline
N-[1-(4-bromophenyl)ethylidene]-2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With C18H5AlF36O4Zn In benzene-d6 at 60℃; for 0.5h; Inert atmosphere; regioselective reaction; | 100% |
With decamethyldizincocene; N,N'-dimethylaniliniumtetrakis(pentafluorophenyl)borate In benzene-d6 at 20℃; for 21.66h; regioselective reaction; | 95 %Spectr. |
With (η1,η5)bis(pentamethylcyclopentadienyl)zinc; N,N'-dimethylaniliniumtetrakis(pentafluorophenyl)borate In benzene-d6 at 60℃; for 0.5h; Inert atmosphere; regioselective reaction; |
2,4,6-trimethylaniline
4-ethynyl-N,N-dimethylaniline
N-[1-(4-(dimethylamino)phenyl)ethylidene]-2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With C18H5AlF36O4Zn In benzene-d6 at 60℃; for 2h; Inert atmosphere; regioselective reaction; | 100% |
With decamethyldizincocene; N,N'-dimethylaniliniumtetrakis(pentafluorophenyl)borate In benzene-d6 at 20℃; for 21.75h; regioselective reaction; | 96 %Spectr. |
With bis(pentamethylcyclopentadienyl)dizinc; N,N'-dimethylaniliniumtetrakis(pentafluorophenyl)borate In benzene-d6 at 20℃; for 21.75h; Inert atmosphere; regioselective reaction; |
3-hydroxy-1(3H)-isobenzofuranone
2,4,6-trimethylaniline
3-(2,4,6-trimethylphenylamino)phthalide
Conditions | Yield |
---|---|
In isopropyl alcohol Reflux; | 100% |
Conditions | Yield |
---|---|
With acetic acid In toluene | 100% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene at 125℃; for 4.5h; Inert atmosphere; Schlenk technique; | 100% |
n-octyne
2,4,6-trimethylaniline
2,4,6-trimethyl-N-(octan-2-ylidene)aniline
Conditions | Yield |
---|---|
With C18H5AlF36O4Zn In benzene-d6 at 60℃; for 2h; Inert atmosphere; regioselective reaction; | 100% |
With C33H49Cl2N2PPd; silver trifluoromethanesulfonate In acetonitrile at 80℃; for 25h; Inert atmosphere; Schlenk technique; | 59% |
With silver hexafluoroantimonate; C25H28Au2Br2N4 In neat (no solvent) at 40℃; for 4h; Inert atmosphere; Schlenk technique; | 76 %Spectr. |
With (η1,η5)bis(pentamethylcyclopentadienyl)zinc; N,N'-dimethylaniliniumtetrakis(pentafluorophenyl)borate In benzene-d6 at 20℃; for 4h; Inert atmosphere; regioselective reaction; |
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylaniline With 15-crown-5; sodium hydride In benzene at 40 - 50℃; for 0.25h; Stage #2: chloroform In benzene at 40℃; for 1h; | 100% |
With benzyltriethylammonium chloride; sodium hydroxide In dichloromethane; water for 22h; | 53% |
2,4,6-trimethylaniline
4-methoxyphenylacetylen
N-(1-(4-methoxyphenyl)ethylidene)-2,4,6-trimethylaniline
Conditions | Yield |
---|---|
With C18H5AlF36O4Zn In benzene-d6 at 60℃; for 6h; Inert atmosphere; regioselective reaction; | 100% |
With silver hexafluoroantimonate; AuBr(8-Mes) In acetonitrile at 90℃; for 14h; Schlenk technique; Sealed tube; | 98% |
With (THT)Au(P(C3H7)2CB11Cl11) In neat (no solvent) at 50℃; for 24h; Catalytic behavior; | 93% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 12h; | 100% |
With air In ethanol at 20℃; for 4h; |
ferrocenecarboxaldehyde
2,4,6-trimethylaniline
Conditions | Yield |
---|---|
In chloroform soln. of Fe-complex and ligand in CHCl3 was heated under reflux, cooled to room temp.; solvent was evapd., dried under vac.; elem. anal.; | 99.62% |
With toluene-4-sulfonic acid In toluene Reflux; Dean-Stark; | 90% |
In chloroform refluxing (6 h); removal of solvent, trituration with hexane; | 82% |
In ethanol boiling; | |
In toluene for 8h; Inert atmosphere; Reflux; Molecular sieve; |
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