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CAS No.: | 131826-11-4 |
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Name: | 3-Isobutylaniline |
Molecular Structure: | |
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Formula: | C10H15N |
Molecular Weight: | 149.236 |
Synonyms: | 3-isobutylphenylamine;3-Isobutylaniline;3-sek.Butyl-anilin; |
Density: | 0.944±0.06 g/cm3(Predicted) |
Boiling Point: | 245.7±9.0 °C(Predicted) |
PSA: | 26.02000 |
LogP: | 3.04850 |
1-(2-methyl-1-propenyl)-3-nitrobenzene
3-isobutylaniline
Conditions | Yield |
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With sodium hypophosphite monohydrate; palladium on activated charcoal; sodium carbonate In acetic acid butyl ester; water for 3h; Reagent/catalyst; Reflux; | 93% |
With hydrogenchloride; palladium on activated carbon In methanol; sodium hydrogencarbonate; ethyl acetate |
3-isobutylaniline
Conditions | Yield |
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Inert atmosphere; |
3-Chloronitrobenzene
3-isobutylaniline
Conditions | Yield |
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Multi-step reaction with 2 steps 1: (η3-allyl)(N,N'-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene)chloropalladium(II); sodium carbonate / acetic acid butyl ester / 5 h / 160 °C / Autoclave 2: sodium hypophosphite monohydrate; palladium on activated charcoal; sodium carbonate / acetic acid butyl ester; water / 3 h / Reflux View Scheme |
3-Bromonitrobenzene
3-isobutylaniline
Conditions | Yield |
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Multi-step reaction with 2 steps 1: palladium diacetate; tri tert-butylphosphoniumtetrafluoroborate; sodium carbonate / acetic acid butyl ester / 10 h / 140 °C / Autoclave 2: sodium hypophosphite monohydrate; palladium on activated charcoal; sodium carbonate / acetic acid butyl ester; water / 3 h / Reflux View Scheme | |
Multi-step reaction with 2 steps 1: palladium diacetate; 1,1'-bis-(diphenylphosphino)ferrocene; sodium carbonate / acetic acid butyl ester / 5 h / 140 °C / Autoclave 2: sodium hypophosphite monohydrate; palladium on activated charcoal; sodium carbonate / acetic acid butyl ester; water / 3 h / Reflux View Scheme |
m-amino isobutyrophenone
3-isobutylaniline
Conditions | Yield |
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With hydrazine hydrate; potassium hydroxide In diethylene glycol at 105 - 180℃; for 8h; Temperature; |
3-bromoaniline
3-isobutylaniline
Conditions | Yield |
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Multi-step reaction with 2 steps 1: potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / water; 1,4-dioxane / 12 h / 100 °C / Inert atmosphere 2: palladium 10% on activated carbon; hydrogen / 1 h / 25 °C / 2585.81 Torr View Scheme |
3-(2-methylprop-1-en-1-yl)aniline
3-isobutylaniline
Conditions | Yield |
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With palladium 10% on activated carbon; hydrogen at 25℃; under 2585.81 Torr; for 1h; |
perfluoroisopropyl iodide
3-isobutylaniline
3-isobutyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline
Conditions | Yield |
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With sodium dithionite; tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate In tert-butyl methyl ether; water at 20℃; | 60% |
With sodium dithionite; tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate In tert-butyl methyl ether; water at 20℃; | 47% |
3-isobutylaniline
1-bromo-3-isobutylbenzene
Conditions | Yield |
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With copper(I) bromide In hydrogen bromide |
3-isobutylaniline
3-isobutyl-4-[1-methoxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]aniline
Conditions | Yield |
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Multi-step reaction with 2 steps 1: tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate; sodium dithionite / water; tert-butyl methyl ether / 20 °C 2: methanol / 5 h / Reflux View Scheme |