2.2- Dimethyl-1 -dimethylamino

Reaktion von 3-Arylsulfinyl-2,2-dimethyl-1-dimethylamino-cyclopropan mit Alko-holen und anschlieBende Hydrolyse408 ... 

For the detection of ionic species other than protons, it is necessary to introduce receptor molecules which can selectively bind guest species on top of the gate of the ISFET. Direct attachment of ion-selective moieties to the surface, e.g. by silylation with (3-cyanopropyl)dimethyl(dimethylamino)silane resulted in some sensitivity towards Ag+ ions (20 mV decade" ), but the sensor was still sensitive towards protons (15 mV decade" ) [10]. Chemical grafting with ammonium phosphonate (1-3) and phosphate sites (4) (Figure 2) or with phthalocyanine-based ionophores bearing crown-ether moieties resulted in a sensitivity towards alkaline (earth) ions, but the pH dependency remained [11,12]. 

Synonyms Aniline, N,N-dimethyl Benzenamine, N,N-dimethyl- (Dimethylamino) benzene N-Dimethylaniline N,N-Dimethylbenzene-amine Dimethylphenylamine N,N-Dimethylphenylamine DMA Xyli-dine... 

Napthyl dimethyl (dimethylamino) silane (preparation). A10% solution of 1 equiv monochlorosilane (naphthyl dimethyl chlorosilane) in hexane (in benzene if necessary for solubility reasons) is stirred in a flask equipped with a reflux condenser cooled at -20 °C. From a communicating flask 2.2 equiv of dimethylamine vapour is slowly introduced over the solution and the mixture kept at room temperature overnight. After filtration and evaporation of the solvent, the residue is distilled. 

A 1,2 dimethoxyethane solution of the PEG is silylated with naphthyl dimethyl dimethylamino-silane. After some working up the extract is dissolved in ethanol and the chromophore concentration evaluated spectrophotometrically. The method is calibrated against PEG of known equivalent weight. 

Figure B2.4.1. Proton NMR spectra of the -dimethyl groups in 3-dimethylamino-7-methyl-l,2,4-benzotriazine, as a fiinction of temperature. Because of partial double-bond character, there is restricted rotation about the bond between the dunethylammo group and the ring. As the temperature is raised, the rate of rotation around the bond increases and the NMR signals of the two methyl groups broaden and coalesce.

This preparation illustrates the use of dimethyl sulphate to convert a primary amino group into the secondary monomethylamino group, without the methy-lation proceeding to the tertiary dimethylamino stage. The methylation of anthranilic acid is arrested at the monomethylamino stage by using i-i molecular equiN alents of sodium hydroxide and of dimethyl sulphate. The reactions can be considered as ... 

Dimethyl-l-phenyl-3-pyrrolyl)vinyl]-6-dimethylamino-l-methylquinolimumpamoate [3546-41-6]... 

Methylisoxazole (297 R = Me) and its homologs can be synthesized by reaction of hydroxylamine hydrochloride with 1-alkyl-3-dimethylamino-2-propen-l-one (296) (54IZV47), the anilino derivatives of acetoacetaldehyde (47G556), 3-dimethyl-aminomethylene-l-propyne (equation 7) (69ZOR1179) and the /3-ketoaldehyde (293) (66JOC3193). 

Cyclization of 3,3-dimethyl-2-hydroximino-4-tosyloxybutane (272) with 1,6-bis-(dimethylamino)naphthalene is reported to occur via iV-alkylation to give the 1-azetine Af-oxide (273) as an unstable oil which decomposes over a few days at room temperature (74TL4283). 

Purine, 1,6-dihydro-8,9-dimethyl-6-thioxo-synthesis, 5, 583 Purine, 2,6-dimethoxy-synthesis, 5, 596 Purine, 2,6-dimethoxy-7-methyl-rearrangement, 5, 558 Purine, 2,7-dimethyl-halogenation, 5, 547 Purine, 7,9-dimethyl-UV spectra, 5, 517 Purine, 8,8-dimethyl-synthesis, 5, 580 Purine, 6-dimethylamino-mass spectra, 5, 519 occurrence, 5, 600 Purine, 6-dimethylamino-9-benzyl-alkylation, 5, 531 Purine, 3,7-dimethyl-6,8-dioxo-methylation, 5, 534 Purine, 6,8-dioxo-alkylation, 5, 534... 

Pyridin-4-one, 3,5-dichloro-2,6-dimethyl-tautomerism, 2, 111 Pyridin-4-one, 1,4-dihydro-polymers, 1, 297 Pyridin-4-one, 2-dimethylamino-synthesis, 2, 419... 

MA -Dimethylamino)phenyl]-2-ethylpropenal (5) was produced by reaction of A, A -dimethyl-aniline (/) with 2-ethyl-3-ethoxyacrolein (2) in the presence of phosphorus oxytrichloride. 

This procedure is based on the method of Lindsay and Hauser as modified slightly by Osgerby and Pauson. N,N-dimethyl-aminomethylferrocene methiodide has also been prepared by heating formylferrocene with dimethylamine and hydrogen in the presence of Raney nickel catalyst to give dimethylamino-methylferrocene, which was quaternized with methyl iodide. ... 

A reagent more reactive than tris(dimethylamino)arsine employed by Weingarten and White 39) was tetrakis(dimethylamino)titanium (145). With this compound it was possible to prepare N,N-dimethyl(l-isopropyl-2-methylpropcnyl)amine (147) from diisopropyl ketone. Weingarten and White 39) have suggested a possible mechanism for this reaction (see p. 88). If benzaldehyde 39,111), formaldehyde 111), or acetaldehyde 39) is used, the corresponding gem diamine or aminal (143) is formed. 

Fulvene-type enamines, which possess some nonbenzenoid aromatic character, have been synthesized by treating cyclopentadienylsodium with an amide-dimethyl sulfate eomplex (117aJ17b) or quaternary pyridinium salts (117c). One of the simplest ones produced is 6-(dimethylamino)fulvene (117a,117d). 

In the case of enamines derived from aldehydes a cycloaddition to give a cyclobutane occurs (48-50). Thus the enamine (16) reacted with methyl acrylate in acetonitrile to give a 91 % yield of methyl 2-dimethylamino-3,3-dimethylcyclobutane carboxylate (56). Similarly, treatment of (16) with diethylmaleate at 170° gave a 70% yield of diethyl 4-dimethylamino-3,3-dimethyl-l,2-cyclobutanedicarboxylate (57), and 16 and acrylonitrile gave a 65% yield of 2-dimethylamino-3,3-dimethylcyclobutanecarbonitrile (58). 

Arylation of enamines with p-benzoquinones takes a somewhat different course (70). The enamine (16) reacts exothermally with p-benzoquinone in benzene solution to give 2-(dimethylamino)-2,3-dihydro-3,3-dimethyl-5-benzofuranol (92). The reaction of enamines with quinone dibenzenesul-fonimide proceeds similarly (68). The product from the enamine (28) is the tetrahydrocarbazole derivative (93). 

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