Copper II acetate

In the flask were placed 60 g of powdered paraformaldehyde, 100 ml of dioxane and 3 g of copper(II) acetate and 0.3 mol of liquid dimethylamine was added at -20 C. The temperature was allowed to rise gradually to 40-45°C with occasional cooling and when the reaction had subsided, the mixture was cooled to 20°C and a second portion of 0.3 mol of the amine was added. When this had reacted, the remainder of the 2.0 mol of dimethylamine was added in the same way. The mixture... 

Stereoselective cis-dihydroxylation of the more hindered side of cycloalkenes is achieved with silver(I) or copper(II) acetates and iodine in wet acetic acid (Woodward gly-colization J.B. Siddall, 1966 L. Mangoni, 1973 R. Criegee, 1979) or with thallium(III) acetate via organothallium intermediates (E. Glotter, 1976). In these reactions the intermediate dioxolenium cation is supposed to be opened hydrolytically, not by Sn2 reaction. 

FLUORINECOMPOUNDS,INORGANIC - BORON - FLUOROBORIC ACID] (Vol 11) Copper(II) acetate [142-71-2]... 

Similarly, hydantoins can be arylated at N-3. For example, treatment of 5,5-diphenyIhydantoin (4), R = R = Cg (phenytoin), with -tolyUead triacetate in the presence of sodium hydride and a catalytic amount of copper(II) acetate (37) gives compound (7). 

Dipping solution Dissolve 3g copper(II) acetate in 100 ml 8-15% aqueous phosphoric acid. 

Figure 28.7 (a) Dinuclear structure of copper(II) acetate, and (b) spin singlet (25 +1 = 1) and spin triplet (25 +1=3) energy levels in dinuclear Cu carboxylates. 

Further oxidation of the carbon at position 21 is interestingly consistent with antiinflammatory activity. Thus oxidation of flucinolone with copper (II) acetate... 

Cupri-. cupric, copper(II). -azetst, n. cupric acetate, copper(II) acetate, -carbonat, n. cupric carbonate, copper(II) carbonate, -chlorid, n. cupric chloride, copper(II) chloride. -hydroxyd, n. cupric hydroxide, cop-per(II) hydroxide. -ion, n. cupric ion, copper(II) ion. -ozalat, n. cupric oxalate, copper(II) oxalate, -oxyd, n. cupric oxide, copper(II) oxide. -salz, n. cupric salt, copper(II) salt, -suifat, n. cupric sulfate. copper(II) sulfate, -sulfid, n. cupric sulfide, copper(II) sulfide, -verbihdung, /. cupric compound, copper(II) compound, -wein-saure, /. cupritartaric acid. 

The formation of porphyrins from 1,19-dideoxybi)enes-/r can be achieved starting either from the 1-methyl derivatives or from l,19-dideoxybilene-Z>-l,19-dicarboxylic acid esters. In the first case the desired methine bridge of the porphyrin stems from the 1-methyl group whereas in the latter case orthoformates have to be added in the condensation step as a precursor for the methine unit. The 1-methyl- and also 1,19-dimethyl-l,19-dideoxybilene- > salts can be cy-clized to the corresponding porphyrins with copper(II) acetate in methanol.56 However, when the bilenes contain /i-acceptor substituents, the yields of porphyrins obtained by this method are very low.57... 

A completely different concept13 makes use of a highly reduced bilane 5 which is oxidatively cyclized to an isobacteriochlorin 6 with copper(II) acetate. The ring closure is initiated by ester cleavage with trifluoroacetic acid and decarboxylative formylation with trimethyl orthoformate to yield a dialdehyde. One of the aldehyde functions forms the desired methine bridge whereas the other is lost during cyclization. 

Due to its commercial importance, the synthesis of copper phthalocyanine (PcCu) is the best investigated of all the phthalocyanines. Copper phthalocyanine is prepared from phthalonitrile and copper(I) chloride without solvent137 and also in a melt of urea.229,277 Additionally, the insertion of copper into metal-free phthalocyanine in butan-l-ol and pentan-l-ol is possible. The copper salts used in this case are copper(I) chloride112 and copper(II) acetate.290 Starting from copper(II) acetate, copper phthalocyanine can also be prepared in ethylene glycol.127 As mentioned above, copper phthalocyanine often occurs as a byproduct of the Rosenmund-von Braun reaction. To increase the yield of the phthalocyanine the solvent dimethylformamide can be substituted by quinoline. Due to the higher boiling point of quinoline, the copper phthalocyanine is the main product of the reaction of copper(I) cyanide and 1,2-dibromoben-zene.130... 

There have been relatively few detailed kinetic studies of the decompositions of metal acetates, which usually react to yield [1046] either metal oxide and acetone or metal and acetic acid (+C02 + H2 + C). Copper(II) acetate resembles the formate in producing a volatile intermediate [copper(I) acetate] [152,1046,1047]. 

SO2CI2) or with I2 and silver acetate. Enol acetates have been regioselec-tively iodinated with I2 and either thallium(I) acetateor copper(II) acetate. ot,P-... 

Free-radical acyloxylation of aromatic substrates has been accomplished with a number of reagents including copper(II) acetate,benzoyl peroxide-iodine, silver(II) complexes, and cobalt(III) trifluoroacetate. ... 

The combination of copper salts and snlfnric acid is another widely used charring reagent. For preparation, 10 ml of concentrated H2SO4 has to be mixed carefully with 90 ml of acetic anhydride. Three grams of copper-II-acetate is dissolved in 100 ml of 8% phosphoric acid. After plate dipping or plate spraying, 15 min of heating at 125°C is recommended [17]. 

Determination of the catalytically active species derived from 1 in solution. Spectrophotoraetric titration of the backbone ligand 5 with copper(II) acetate in methanol revealed formation of a dinuclear copper(ll) complex species Cu2L.3h(OAc) above a 1 2 molar ratio. A mononuclear copper(ll) species CuL 2h (6) dominates at a 1 1 molar ratio of 5 and copper(ll) acetate. Control experiments for the assignment of putative structures based on the obtained spectroscopic data included a UVA is spectroscopic titration of 5 with anhydrous sodium acetate in the presence of copper(ll) chloride and revealed that acetate is necessary for the formation of a copper (11) complex in methanol. The composition of 1 in methanol is the same as determined by elemental analysis for the sohd state. 

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