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Ethyl-«-butylamine

Ethyl bromoacetate, 21, 51 23, 37 Ethyl o-bromoglutaconate, 26, 44 Ethyl a-bromoisobutyrate, 21, 53 Ethyl 8-beomopropionate, 20, 6S Ethyl- -butylamine, 25, 19 Ethyl -butylcyanoacetate, 26, 31 Ethyl caprylate, 20, 69 Ethyl ff-carbethoxy-(3-w-chloroanilino-acrylate, 28, 39... [Pg.53]

Hexamethylenediamine lWb uylamine 4> Oxy-ethylated butylamine Oxy-ettuiated aniline Substituted pipeiazone Substituted pyrrolidine ) Substituted > idine ) Triazds ) Substituted benziroidazols Pobrvinyl pyridine )... [Pg.107]

Synonyms 1-Butanamine, N-ethyl- Butylamine, N-ethyl- Butylethylamine N-Ethyl-1-butanamine Ethylbutylamine N-Ethyibutylamine N-Ethyi-1-butylamine N-Ethyi-N-butyiamine Empirical CeHisN... [Pg.1694]

Ethyl malonate or n-butylamine Benzyl acetate or diethylcarbitol -160° Isopentane... [Pg.38]

The procedure is illustrative of a general method of ethylating amines, wherein one reacts the amine with ethylene using an alkali-metal salt of the amine as catalyst.2 Di- -butylamine and -hexylamine have been thus ethylated at 130-160°, aniline, o-toluidine, and N-methylaniline at 240-275°. In general, higher olefins add to amines only sluggishly.2... [Pg.47]

Amines can be N-alkylated by reaction with alcohols, in a sealed tube with irradiation by microwaves, with the alcohol and RuCl2(PPh3)2, or by treatment with the amine, SnCl2 and Pd(PPh3)4. Chlorodiethylaluminum (Et2AlCl), with a Cu(ll) catalysts can N-ethylate aniline derivatives. tcrt-Butylamines can be prepared from isobutylene, HBr and the amine by heating a sealed tube. ... [Pg.501]

Reaction of m-chlorobenzonitrile with ethyl Grignard reagent produces ethylarylketone 191. Bromination in methylene chloride followed by displacement of the a-bromoketone moiety with t-butylamine... [Pg.124]

Ethyl maltol, 12 49 Ethylmercuric chloride, 22 25 Ethyl-n-butylamine, 2 538t... [Pg.337]

Despite this superficial similarity, however, subtle differences between the behaviour of ionized amines and the analogous ionized alcohols and ethers remain. Thus, metastable ionized 2-butylamine loses 80% ethane in contrast, ionized 2-butanol eliminates both ethane (35%) and methane (40%)85. The latter reaction corresponds to loss of the smaller methyl group and an a-hydrogen atom from the larger ethyl substituent at the branch point. Methane loss does not occur from ionized amines with a methyl substituent on the -carbon, with the solitary exception of ionized isopropylamine which does expel methane (10%). However, ionized 3-hexylamine eliminates both ethane (35%) and propane (20%)85. [Pg.218]

When the decomposition of the zwitterionic intermediate is rate-determining, the effect of the solvent is crucial since it may produce changes in the mechanisms and in the rate-determining step. A recent study of the kinetics of the reactions of 1-chloro-, 1-fluoro- and l-phenoxy-2,4-dinitrobenzene with piperidine, n-butylamine and benzylamine in ethyl acetate and THF indicated that these reactions resemble those in dipolar aprotic solvents when primary amines are the nucleophiles (i.e. that shown in equation 1, with... [Pg.1221]

A kinetic smdy of the formation of zwitterionic adducts (28) from 1,3,5-trinitrobenzene and diazabicyclo derivatives indicates that reactions are surprisingly slow, with rate constants many orders of magnitude lower than those for related reactions with primary or secondary amines. The use of rapid-scan spectrophotometry was necessary to study the kinetics of reaction of 4-substimted-2,6-dinitro-A -n-butylanilines (29) with n-butylamine in DMSO the two processes observed were identified as rapid deprotonation to give the conjugate base and competitive a-adduct formation at the 3-position. The reactions of MAf-di-n-propyl-2,6-dinitro-4-trifluoromethylaniline (30), the herbicide trifluralin, and its A -ethyl-A -n-butyl analogue with deuteroxide ions and with sulfite ions in [ H6]DMS0-D20 have been investigated by H NMR spectroscopy. With deuteroxide a-adduct formation at the 3-position is followed by... [Pg.283]

EINECS 203-468-6, see Ethylenediamine EINECS 203-470-7, see Allyl alcohol EINECS 203-472-8, see Chloroacetaldehyde EINECS 203-481-7, see Methyl formate EINECS 203-523-4, see 2-Methylpentane EINECS 203-528-1, see 2-Pentanone EINECS 203-544-9, see 1-Nitropropane EINECS 203-545-4, see Vinyl acetate EINECS 203-548-0, see 2,4-Dimethylpentane EINECS 203-550-1, see 4-Methyl-2-pentanone EINECS 203-558-5, see Diisopropylamine EINECS 203-560-6, see Isopropyl ether EINECS 203-561-1, see Isopropyl acetate EINECS 203-564-8, see Acetic anhydride EINECS 203-571-6, see Maleic anhydride EINECS 203-576-3, see m-Xylene EINECS 203-598-3, see Bis(2-chloroisopropyl) ether EINECS 203-604-4, see 1,3,5-Trimethylbenzene EINECS 203-608-6, see 1,3,5-Trichlorobenzene EINECS 203-620-1, see Diisobutyl ketone EINECS 203-621-7, see sec-Hexyl acetate EINECS 203-623-8, see Bromobenzene EINECS 203-624-3, see Methylcyclohexane EINECS 203-625-9, see Toluene EINECS 203-628-5, see Chlorobenzene EINECS 203-630-6, see Cyclohexanol EINECS 203-632-7, see Phenol EINECS 203-686-1, see Propyl acetate EINECS 203-692-4, see Pentane EINECS 203-694-5, see 1-Pentene EINECS 203-695-0, see cis-2-Pentene EINECS 203-699-2, see Butylamine EINECS 203-713-7, see Methyl cellosolve EINECS 203-714-2, see Methylal EINECS 203-716-3, see Diethylamine EINECS 203-721-0, see Ethyl formate EINECS 203-726-8, see Tetrahydrofuran EINECS 203-729-4, see Thiophene EINECS 203-767-1, see 2-Heptanone EINECS 203-772-9, see Methyl cellosolve acetate EINECS 203-777-6, see Hexane EINECS 203-799-6, see 2-Chloroethyl vinyl ether EINECS 203-804-1, see 2-Ethoxyethanol EINECS 203-806-2, see Cyclohexane EINECS 203-807-8, see Cyclohexene EINECS 203-809-9, see Pyridine EINECS 203-815-1, see Morpholine EINECS 203-839-2, see 2-Ethoxyethyl acetate EINECS 203-870-1, see Bis(2-chloroethyl) ether EINECS 203-892-1, see Octane EINECS 203-893-7, see 1-Octene EINECS 203-905-0, see 2-Butoxyethanol EINECS 203-913-4, see Nonane EINECS 203-920-2, see Bis(2-chloroethoxy)methane EINECS 203-967-9, see Dodecane EINECS 204-066-3, see 2-Methylpropene EINECS 204-112-2, see Triphenyl phosphate EINECS 204-211-0, see Bis(2-ethylhexyl) phthalate EINECS 204-258-7, see l,3-Dichloro-5,5-dimethylhydantoin... [Pg.1482]

Mole-nots, see Strychnine Mollan 0, see Bis(2-ethylhexyl) phthalate Mondur TD, see 2,4-Toluene diisocyanate Mondur TD-80, see 2,4-Toluene diisocyanate Mondur TDS, see 2,4-Toluene diisocyanate Monobromobenzene, see Bromobenzene Monobromobenzol, see Bromobenzene Monobromoethane, see Ethyl bromide Monobromomethane, see Methyl bromide Monobromotrifluoromethane, see Bromotrifluoromethane Monobutylamine, see Butylamine Mono-n-butylamine, see Butylamine Monobutyl ethylene glycol ether, see 2-Butoxyethanol Monochlorbenzene, see Chlorobenzene Monochlorethane, see Chloroethane Monochloroacetaldehyde, see Chloroacetaldehyde Monochlorobenzene, see Chlorobenzene Monochlorodibromomethane, see Dibromochloromethane Monochlorodiphenyl oxide, see 4-Chlorophenyl phenyl ether... [Pg.1496]

See other pages where Ethyl-«-butylamine is mentioned: [Pg.204]    [Pg.447]    [Pg.611]    [Pg.392]    [Pg.636]    [Pg.142]    [Pg.204]    [Pg.447]    [Pg.611]    [Pg.392]    [Pg.636]    [Pg.142]    [Pg.957]    [Pg.376]    [Pg.127]    [Pg.77]    [Pg.26]    [Pg.29]    [Pg.957]    [Pg.113]    [Pg.32]    [Pg.181]    [Pg.43]    [Pg.195]    [Pg.45]    [Pg.584]    [Pg.1218]    [Pg.1244]    [Pg.1250]    [Pg.1253]    [Pg.297]    [Pg.1464]    [Pg.132]    [Pg.132]    [Pg.150]    [Pg.563]   
See also in sourсe #XX -- [ Pg.19 , Pg.25 ]



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Ethyl n-butylamine

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