4- Ethyl-3- - - nitroso

Unter gleichen Bedingungen verlauft die Cyclisierung zu N-Aminocarbonyl-Systemen mit Iso-cyanaten73. Man erhalt z.B. aus [(l-Benzyl-ethyl)-nitroso-amino)-acetonitril mit Phenyl-isocyanat in 88%iger Ausbeute 3-(1-Benzyl-ethyl )-sydnon-(anilinocarbonyl-imin) (Schmp. 132-133°) ... 

The diazepinol (8) has been obtained by treatment of 0-ethyl-nitroso-i 7,i 7-pentamethyleneimmonium fluoroborate (9) with cold 1.5 N sodium carbonate.15... 

Naphthyridin 3-Carboxy-l-ethyf-6-(ethyl-nitroso-amino)-4-oxo-1,4-dihydro- El6a, 794 (N-Nitrosier.)... 

SYNS AETHYLNITROSOURETHAN (GERMAN) ENU ETHYLESTER KYSELINY N-ETHYL-N-NITRO-SOKARBAMINOVE ETHYL N-ETHYLNITROSO-CARBAMATE ETHYLNITROSOCARBAMIC ACID, ETHYL ESTER N-ETHYL-N-NITROSOCARBAMIC ACID ETHYL ESTER ETHYL NITROSOURETH. N N-ETHYL-N-NITROSOURETHAN ETHYL NITROSO-URETHANE N-ETHYL-N-NITROSOURETHANE NEU NITROSOETHYLURETHAN N-NTTROSO-N-ETHYLURETHAN NITROSO-N-ETHYLURETHANE NSC-24890... 

In the present preparation, ethyl acetoacetate is treated with sufficient nitrous acid to convert half into the a-nitroso (or a-oximino) ester, which is reduced by zinc and acetic acid to the a-amino ester (I). The latter then condenses with... 

Secondary and tertiary amines are not generally prepared in the laboratory. On the technical scale methylaniline is prepared by heating a mixture of aniline hydrochloride (55 parts) and methyl alcohol (16 parts) at 120° in an autoclave. For dimethylaniline, aniline and methyl alcohol are mixed in the proportion of 80 78, 8 parts of concentrated sulphuric acid are added and the mixture heated in an autoclave at 230-235° and a pressure of 25-30 atmospheres. Ethyl- and diethyl-anihne are prepared similarly. One method of isolating pure methyl- or ethyl-aniline from the commercial product consists in converting it into the Y-nitroso derivative with nitrous acid, followed by reduction of the nitroso compound with tin and hydrochloric acid ... 

Aziridine, 2,3-diphenyl-l-(2,4,6-trinitrophenyl)-irradiation, 7, 61 Aziridine, 1,2-divinyl-rearrangement, 7, 539 Aziridine, 2,3-divinyl-rearrangement, 7, 42, 65, 539 Aziridine, N-ethyl-inversion, 7, 6 Aziridine, 2-halo-reactions, 7, 74 Aziridine, A/-halo-invertomers, 7, 6 Aziridine, 2-methyl- N NMR, 7, 11 Aziridine, methylene-ring-ring valence isomerizations, 7, 22 synthesis, 7, 92 Aziridine, iV-nitroso-reactions, 7, 74 Aziridine, iV-phosphino-inversion, 7, 7 Aziridine, 1-phthalimido-UV irradiation, 7, 62-63 Aziridine, l-(3-thienyl)-2-vinyl-rearrangement, 4, 746 Aziridine, 7V-trimethylsilyl-inversion, 7, 7 Aziridine, 1,2,3-triphenyl-irradiation, 7, 61 Aziridine, vinyl-isomerization, S, 287 Aziridinecarboxylic acid ring expansion, 7, 262 Aziridine-2,2-dicarboxylic acid, 1-methoxy-diethyl ester... 

Originally, p-tolylsulfonyldiazomethane was prepared by passing an ethereal solution of its precursor, ethyl i 7-nitroso-iV -(j3-toly]8ulfonyI-methyl)carbamate, slowly through a column of alumina, This procedure, which results in yields about 10% higher, is convenient only for small-scale preparations, up to a maximum of 5 g. of p-tolylsulfonyl-diazomethane. The present modification is due to Middelbos, ... 

Benzeneamine, N-hydroxy-N-nitroso,ammonium salt Nitrilotrlacetic acid 4,4 -Thiodianiline Ethyl acrylate Butyl acrylate Ethyleneimine (Aziridine) p-Nrtrosodiphenylamine Calcium cyanamide Hydrazine Aldrin... 

Cyclocondensation of 2-aminopyridines and ethyl cyano(hydroxyimi-no)acetate in the presence of NaOEt gave 4-amino-3-nitroso-4//-pyrido[l,2-n]pyrimidin-2-ones 348 (95JHC1725). 

Condensation of ethyl acetoacetate with phenyl hydrazine gives the pyrazolone, 58. Methylation by means of methyl iodide affords the prototype of this series, antipyrine (59). Reaction of that compound with nitrous acid gives the product of substitution at the only available position, the nitroso derivative (60) reduction affords another antiinflammatory agent, aminopyrine (61). Reductive alkylation of 61 with acetone in the presence of hydrogen and platinum gives isopyrine (62). Acylation of 61 with the acid chloride from nicotinic acid affords nifenazone (63). Acylation of 61 with 2-chloropropionyl chloride gives the amide, 64 displacement of the halogen with dimethylamine leads to aminopropylon (65). ... 

Phenylethvl benzoate from decomposition of N nitroso N (2-phenyl-ethyl)benzamide, 47, 45 Phenylethyny lhthium 46, 88 Phenylethyny lmagnesium, Gngnard reagent, 46, 88... 

Trinitro-N-methylaniline (N-methyl picra-mide), yellow needles from EtOH contg acid, mp /l4.8° (Refs 4 7) the UV spectrum has a peak at 340 and a shoulder at 410—20m (Ref 19) CA Registry No 1022-07-7. It is prepd by the hydrolysis of the N nitroso compd (see below) at 70—80° (Ref 5) by the action of coned sulfuric acid (Ref 8) or UV light (Ref 12) on Tetryl by the action of methyl amine on Ethyl Picrate (Ref 18) or Tetryl (Ref 7) or by the action of nitric acid (d 1.42g/cc) at 0° on N,N-dimethylaniline (Ref 10). It is present in crude Tetryl and is the active der-matitic agent in the latter (Ref 12). It can be isolated from crude Tetryl and identified by thin layer chromatography (Ref 21)... 

N-Nitroso-N-methyl-N -nitroguanidine, diazomethane from, 41, 10 Nitrosomethylurethane, warning because a carcinogen, 43, 86 o-Nitrotoluene, condensation with ethyl oxalate, 43,40... 

Ethyl nitrite, 58,113,115 ETHYL 7-3-NITROACRYLATE, 56,65 Ethyl JV-nitroso-JV-(p-tolylsulfonylmethyl> carbamate, 57, 96 Ethyl nonanoate, 59, 110 Ethyl 7-oxo-l-cycloheptene-l-carboxylate,... 

By this reaction, the nitroso moiety is replaced by a nitro group, in addition to the nitration of the -NH-ethyl group [38]. 

Giomi s group developed a domino process for the synthesis of spiro tricyclic nitroso acetals using a, 3-unsaturated nitro compounds 4-163 and ethyl vinyl ether to give the nitrone 4-164, which underwent a second 1,3-dipolar cycloaddition with the enol ether (Scheme 4.35) [56]. The diastereomeric cycloadducts formed, 4-165 and 4-166 can be isolated in high yield. However, if R is hydrogen, an elimination process follows to give the acetals 4-167 in 56% yield. 

Biacetyl monoxime has been prepared by the action of amyl nitrite on methyl ethyl ketone using sodium hydroxide1 or hydrochloric acid 2 as a condensing agent, and by melting nitroso-levulinic acid.3... 

Nitrooxazoles and 4-nitroisoxazoles 480 are versatile substrates for domino cycloaddition reactions with ethyl vinyl ether 481 to form the tricyclic nitroso acetals 482 and 483 (Equation 129) <1999T13809, 2001T4237>. 

Into a 3-1., three-necked flask (Note 1) equipped with a reflux condenser and an efficient stirrer is placed 11. of absolute (99.8%) ethanol. To this is added 39.4 g. (1.72 g. atom) of sodium metal, and, after solution is complete (Note 2), 91.5 ml. (97.2 g., 0.86 mole) of ethyl cyano-acetate (Note 3) and 51.5 g. (0.86 mole) of urea are added. The mixture is heated under reflux on a steam bath with vigorous stirring for 1 hours. After about 2 hours, the reaction mixture becomes practically solid, and the stirrer may have to be stopped. At the end of the reac-I ion time, 1 1. of hot (80°) water is added to the reaction mixture, and si i rring is resumed. After complete solution has taken place, the stirred mixture is heated at 80° for 15 minutes and is then neutralized to litmus with glacial acetic acid (Note 4). Additional glacial acetic acid (75 ml.) is then added, followed by cautious addition of a solution of 64.8 g. (0.94 mole) of sodium nitrite dissolved in 70 ml. of water. The rose-red nitroso compound separates almost immediately as an expanded precipitate which almost stops the stirrer. After a few minutes the ni-... 

Another research group (147) studied the reaction of vinyl ethyl ether with optically pure a-nitroolefin (302) giving rise to enantiomerically pure nitronate (303). The reaction of the latter with an excess of the olefin gradually produces nitroso acetal (304) (Scheme 3.181). 

N-Methylethylamine has been prepared by heating ethyl-amine with methyl iodide in alcohol at 100° 3 by the hydrolysis of N-methyl-N-ethylarenesulfonamides,4-5 -nitroso-N-methyl-N-ethylaniline,6 or methylethylbenzhydrylidene ammonium iodide 7 by catalytic hydrogenation of ethyl isocyanate or ethyl isocyanide 8 and by the reduction of ethyl isocyanate by lithium aluminum hydride,9 of N-methylacetisoaldoxime by sodium amalgam and acetic acid,10 or of a nitromethane/ethylmagnesium bromide adduct by zinc and hydrochloric acid.11... 

Ethyl acetoaoetate /.so-nitroso-derivative of ethyl aoetoacetate... 

Dimethylaminoazobenzene Ethyl diazoacetate Ethylenethiourea Ethyl iV-nitroso carbamate ... 

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