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Nitro compds alcohols

C2H5.C02.CH2.CH(N02).CH3 mw 161.18 N 8.69% OB to C02 -134.00% colorl liq mp, when heated over 150° the compd deton , bp 106.8 to 107.0° at 10mm d 1.1201g/cc RI 1.42815. Prepn is by reacting at a boil 2-nitro-propyl alcohol with propionic acid using benz as the solvent, and coned sulfuric acid as the coupling reagent. The prod is recovered by vac distn... [Pg.954]

Janovsky Test. Color reactions produced by treating aromatic nitro compds with hot" cold alcoholic NaOH or KOH and acetonic NaOH solns. A table of color reactions of some nitro compds is given in Ref 2. See Janovsky s Reagent under COLOR REACTIONS and COLOR REAGENTS in Vol 3 of Encycl, p C405-R... [Pg.451]

Dynamit-Nobel AG, NethP, Appl 6411854 (1966) CA 65, 6992(1966) (Liquid esters of nitric acid and aromatic nitro compds can be gelatinized with polymers of unsatd acids or unsatd alcohols and their derivs. The advantages of these polymers include increased safety of manipulation and increased rate of gelatinizacioii. Thus a 60/40—NG/ NGc soin was mixed with 3 wt %-of finely powd polymethylacrylates and, after 1.5 hrs, had a viscosity of 4250 cp at 20° under shearing gradient of 15 sec )... [Pg.567]

Piperidine. Hexahydropyridine. CjH N mol wt 85.15. C 70.52%, H 13.02%, N 16.45%. Found in small quantities in Piper nigrum L.. Piperaceae (black pepper). May be obtained from pipeline by henting with alcoholic KOH, or from 1,5-diaminopentane hydrochloride by cycli-zarion. Usually prepd by electrolytic reduction of pyridine. Forms complexes with salts of heavy metals. Because of its reactivity, piperidine is useful in the prepn of cryst derivatives of aromatic nitro compds contg nuclear halogen atoms Seikel, J, Am. Chem. Soc. 62, 750 (1940). Review of physical constants of piperidine and N-alkyl piperidines Magnus -... [Pg.1186]

USE For prepn of standard NaNOj soln for water analy -sis prepn of aliphatic nitro-compds as reagent for primary, secondary, and tertiary alcohols. [Pg.1349]

Uses Catalyst for dehydrogenation of alcohols, decomposition of methanol, oxygen scavenging, dehydrogenation of piperazines to pyrazines, hydrogenation of fatty acids and esters, aldehydes, ketones, unsat. alcohols, aromatic nitro compds. [Pg.1038]

Classification Aliphatic nitro compd. nitroparaffin Empirical C3H7NO2 Formula CH3CH(N02)CH3 Properties Colorless to very It. yel. clear oily liq. mild fruity odor sol. in most aromatic hydrocarbons, alcohols, esters, ketones, chloroform, ethers, lower carboxylic acids si. sol. in water m.w. 89.09 sp.gr. 0.992 (20/20 C) vapor... [Pg.2836]

Alcohols from oxo compds. 20 eqs. NaBH4 added to a soln. of 5 eqs. ZrC in THF at room temp, under N2, a soln. of 4 eqs. acetophenone in the same solvent added, and the mixture stirred at room temp, for 5 h - 1-phenylethanol. Y 96%. ZrCl4 is inexpensive, easy to use, and does not affect ar. nitro compds. and bromides. F.e., also reduction of carboxylic acids, esters and halides to prim, alcohols, and amides, oximes, alkoximes, nitriles, and imines to amines, s. S. Itsuno et al.. Synthesis 1988, 995-6. [Pg.24]

Ozone dimethyl sulfide-sodium alcohol Oxo from aliphatic nitro compds. [Pg.67]

A convenient one-step conversion of aromatic nitro compds. to phenols with benzaldoxime has been reported High yields of alcohols, ethers, carboxylates, and nitrates can be obtained from alkyl halides with mercury salts... [Pg.309]

Lower valent tungsten halides are a new class of deoxygenation agents, e.g. for the conversion of carbonyl or epoxy compounds into olefins . A new reagent, generated in situ from iron pentacarbonyl and a small amount of base in moist solvents, selectively and efficiently hydrogenates the ethylenic portion of a,/ -unsaturated carbonyl compounds, such as ketones or lactones, under mild conditions. Aliphatic tert. amides can be easily reduced to alcohols by alkali metals in hexa-methylphosphoramide and a protic cosolvent such as tert-butanol. Aldehydes can be obtained from acids by catalytic reduction of intermediate carboxylic alkoxyformic anhydrides . Sec. nitro compds. are converted into ketones by the joint action of a nitrite ester and NaNOg under mild, non-acidic conditions . [Pg.9]

A mixture of 2,4,6-triphenylthiopyrylium perchlorate, malononitrile, diisopropyl-ethylamine, and alcohol refluxed 1 hr. 2,4,6-triphenylbenzonitrile. Y 72%. F. e. s. G. A. Reynolds and J. A. Van Allan, J. Heterocyclic Chem. 8, 301 (1971) with K-f rf-butoxide in tert-buianol, different products from nitro compds. depending on work-up, s. Z. Yoshida et al.. Tetrahedron 27, 6083 (1971). [Pg.208]

Potassium hy dr oxide alcohol Nitrones from ar. nitro compds. [Pg.515]

Ozoneldimethy I sulfide-sodium/alcohol Oxo from aliphatic nitro compds. s. 29,199 s. a. Org. Synth. 56,36 (1977)... [Pg.360]

By March 1, 1957, the ami noethylation of the following materials and compds had been achieved by the Wyandotte Chemicals Corp cellulose, cellulose derivatives, regenerated c e 1 lu los e, 2-hydroxymethy 1-2-nitro-1,3-pro-panediol, nylon, polyurethane, polyvinyl alcohol, polyvinylchloride, protein(wool), starch and toluene diisocyanate... [Pg.202]

Bactericides -arsenic compds as [ARSENIC COMPOUNDS] (Vol 3) -coordination compounds as [COORDINATION COMPOUNDS] (Vol 7) -in iodine production [IODINE AND IODINE COMPOUNDS] (Vol 14) -frommtro alcohols [NITRO ALCOHOLS] (Vol 17) -use of acetic anhydride [ACETIC ACID AND DERIVATIVES - ANHYDRIDE] (Vol 1)... [Pg.85]

UV irradiation of aq solns of TNT has yielded a mixt of products, 15 of which have been identified (Ref 85). The methyl group has undergone reaction in all of these compds (to alcohol, aldehyde, carboxyl, or their derivatives). A nitro group has reacted in some cases this is always ortho and never para to the methyl group. Reaction of TNT which involve the intermediacy of anion (D), such as the reaction with 4-nitroso-... [Pg.749]


See other pages where Nitro compds alcohols is mentioned: [Pg.62]    [Pg.251]    [Pg.188]    [Pg.251]    [Pg.187]    [Pg.62]    [Pg.251]    [Pg.251]    [Pg.188]    [Pg.200]    [Pg.567]    [Pg.583]    [Pg.62]    [Pg.251]    [Pg.940]    [Pg.488]    [Pg.823]    [Pg.125]    [Pg.52]    [Pg.601]    [Pg.889]    [Pg.125]    [Pg.125]    [Pg.489]    [Pg.824]    [Pg.125]    [Pg.125]    [Pg.602]   
See also in sourсe #XX -- [ Pg.29 ]




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Nitro compds

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