Propylamine, 1,1-Dimethyl

Dimethyl propanoic acid, AE74 Dimethyl propylamine, AF05... 

Commercial 3-chloro-W.W-dimethyl propylamine hydrochloride (Michigan Chemical Corporation, 351 E. Ohio St., Chicago, 111. 60611) was added to cold (0°C.), saturated... 

Dimethyl propylamine dimethametryn 3 Dimethyl propylamine propamocarb Dimethyl sulfamoyl chloride bupirimate... 

C7H17N dimethyl-1,2-dimethyl propylamine 66225-38-5 190.00 16.907 2 14093 C8H11N m-ethyl aniline 587-02-0 209.15 12.600 2... 

Beilstein Handbook Reference) AI3-25441 1-Amino-3-dimethylaminopropane BRN 0605293 CCRIS 4799 EINECS 203-680-9 HSDB 5391 1-(Dimefhylamino)-3-aminopropane 3-(Dimethylamino)-propylamine y-(Dimethylamino)propylamine N,N-Di-methyl-1,3-diaminopropane NSC 1067 1,3-Propane-diamine, N,N-dimethyl- Propylamine, 3-(N,N-dimethyl-amino)-. 

Butanamine, N-ettiyl-3-methyl- N-Ethyl-1,2-dimethyl-propylamine N-Ethyl-3-methyl-2-butanamine Propyl-amine, N-ethyl-1,2-dimethyl-,... 

Synenyms 1-Amlno-3-dlmethylamlnopropane 3-Amlnopropyldlmethylamlne N,N-Dlmelhyl-1,3-amlnopropane 3-Dlmethylamlnopropylamlne N,N-Dlmethylamlno-propylamlne N,N-Dlmethyl-N-(3-amlnopropyl) amine N,N-Dlmethyl-1,3 lamlno-propane N,N-Dlmelhyl-1,3-propanedlamlne N,N-Dlmelhyl-1,3-propylenedlamlne DMAP DMAPA 1,3-Propanediamine, N.N-dimethyl- Propylamine, 3-(N,N-dlmethylamlno)-Ciassificatien Nonaromatic amine Empiricai CjH,4N2 Fermuia (CH3) CH2CH2CH2NH2... 

Diaminobiphenyl Derivative, 698 /7-Propylamine and /-Propylamine Derivatives, 699 /V,/ /-Dimethyl-(f ,/ )-1,2-diaminocyclohexyl, 699 Morpholine Derivative, 699... 

The Leuckart synthesis has been applied successfully in the thiophene series, iV,A -Dimethyl thenylamine and A, A -diethyl thenylamine were obtained from 2-thiophenealdehyde and the appropriate for-mamide. Seven -(2-thienyl)- -arylethylamine hydrochlorides have been prepared from the corresponding ketones in about 40-60% yields and, finally, A -methyl-1-(3-thienyl)-2-propylamine was obtained in 48% yield in the Leuckart reaction from 3-thienylace-tone, methylamine, and formic acid. ... 

Constitutional isomerism is not limited to alkanes—it occurs widely throughout organic chemistry. Constitutional isomers may have different carbon skeletons (as in isobutane and butane), different functional groups (as in ethanol and dimethyl ether), or different locations of a functional group along the chain (as in isopropylamine and propylamine). Regardless of the reason for the isomerism, constitutional isomers are always different compounds with different properties, but with the same formula. 

Propanol with magnesium in reduction of chlorobenzene, 47, 104 Propionyl fluoride, 46, 6 n Propylamine, 46, 85 n Propylhydrazine, 46, 85 C ( Propyl) N phenylmtrone, genera tion from phenylhydroxylamme and n butyraldehyde, 46, 97 Purification of tetrahydrofuran (Warning), 46,105 4H Pyran 4-one, 2 6 dimethyl 3,5 diphenyl, 47, 54... 

Piopionitrile, 2,3,3-triphenyl [Propanem tnle, 2,3,3-tnphenyl-], 55, 94, 102 Propylamine, 3-chloro-JV,/V-dimethyl- [ 1-... 

Propylamine, 3 chloro A, TV dimethyl ], hydrochloride, 55, 128 1-PROP AN AMINE, 3,3 -(phenylphosphini-denc)bis(A, A -dimethyl)- [Phosphine, phenyl-, bis(3-dimethylammopro-... 

A variety of cleavage conditions have been reported for the release of amines from a solid support. Triazene linker 52 prepared from Merrifield resin in three steps was used for the solid-phase synthesis of aliphatic amines (Scheme 22) [61]. The triazenes were stable to basic conditions and the amino products were released in high yields upon treatment with mild acids. Alternatively, base labile linker 53 synthesized from a-bromo-p-toluic acid in two steps was used to anchor amino functions (Scheme 23) [62]. Cleavage was accomplished by oxidation of the thioether to the sulfone with m-chloroperbenzoic acid followed by 13-elimination with a 10% solution of NH4OH in 2,2,2-trifluoroethanol. A linker based on l-(4,4 -dimethyl-2,6-dioxocyclohexylidene)ethyl (Dde) primary amine protecting group was developed for attaching amino functions (Scheme 24) [65]. Linker 54 was stable to both acidic and basic conditions and the final products were cleaved from the resin by treatment with hydrazine or transamination with ra-propylamine. 

Analogous products are obtained if 2-fury lmethylamine, di-n-propylamine, or -(1,5-dimethyl)hexylamine are used instead of NH3, with yields of 67, 88 and 84%, respectively. 

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