Acrolein dichloride

The desired intermediates, a pentadienol or a pentenetriol were unknown at the time, but it occurred to me that their synthesis might be accomplished by the partial reduction of a pentenynol or a pentynetriol, the latter being obtained from the reaction of one molecule of acrolein or acrolein dichloride with the Grignard reagent derived from acetylene. The reactions which have been carried out in accordance with this scheme are shown in the accompanying flow sheet. 

Recently, Diels-Alder reactions between cyclopentadiene and menthoxyaluminum dichloride-acrolein complexes were investigated by means of combined AM1/AM3 calculations and the results were compared to full AMI results211. 

Density functional theory has been used to investigate the Diels-Alder reactions of triazolinedione with s-cis- and. y-fran -butadiene. " Combined quantum mechanics-molecular mechanics calculations have been used to investigate the asymmetric Diels-Alder reaction of cyclopentadiene with the complex dienophiles AICI3-methyl acrylate and methoxyaluminium dichloride-acrolein.Equilibrium constants have been determined for the molecular complexes formed from 1-alkyl-1-(2-naphthyl)ethenes and 1-vinylnaphthalene with TCNE in C1(CH2)2C1 at 27.1 °C ... 

Propylbenzene, see Propylbenzene Propyl carbinol, see 1-Butanol Propylene aldehyde, see Acrolein, Crotonaldehyde Propylene chloride, see 1,2-Dichloropropane Propylene dichloride, see 1,2-Dichloropropane a,p-Propylene dichloride, see 1.2-Dichloropropane 1,2-Propylene oxide, see Propylene oxide Propyl ester of acetic acid, see Propyl acetate Propylethylene, see 1-Pentene 5-Propylhexane, see 4-Methyloctane Propyl hydride, see Propane Propylic alcohol, see 1-Propanol Propyl iodide, see 1-Iodopropane n-Propyl iodide, see 1-Iodopropane Propylmethanol, see 1-Butanol Propyl methyl ketone, see 2-Pentanone n-Propyl nitrate, see Propyl nitrate... 

In 1979, Koga and coworkers disclosed the first practical example of a catalytic enantioselective Diels-Alder reaction [44] promoted by a Lewis acidic complex, presumed to be menthoxyaluminum dichloride (1), derived from menthol and ethylaluminum di chloride, whose structure remains undefined [45]. This complex catalyzed the cycloaddition of cyclopentadiene with acrolein, methyl acrylate, and methacrolein with enantioselectivities as high as 72% ee. Oxidation of 2 (predominantly exo) followed by recrystallization actually lowered the ee ... 

Addition (See also Michael reaction. Thiele reaction.) Acrolein. Cuprous chloride. Cuprous iodide. Diethylaluminum cyanide. Difluoramine. Dimethylcopper lithium. Methyl(tri-K-butylphosphine)copper complex. Methyl vinyl ketone. Rhodium trichloride. Sulfur dichloride. 

IRON DICHLORIDE (7758-94-3) Contact with ethylene oxide may initiate polymerization. Reacts violently with reducing agents, acrolein, alcohols, chlorine trifluoride, ethers, fluorine, hydrazine, hydrazinium perchlorate, hydrogen peroxide, finely divided aluminum or magnesium, peroxyfuroic acid, sodium acetylide. Sensitizes most organic azides that are unstable shock and heatexplosives. Forms explosive materials with 1,3-di(5-tetrazoyl)triazene, potassium, sodium. Incompatible with glycidol, isopropyl chlorocarbonate, nitrosyl perchlorate, sodium borohydride. Aqueous solution attacks metals. 

ISOTHIOUREA (62-56-6) Aqueous solution is a base. Violent reaction with acrolein, strong acids. Incompatible with acrylaldehyde, hydrogen peroxide, metal salts. Aqueous solution incompatible with organic anhydrides, acrylates, alcohols, aldehydes, alkylene oxides, substituted allyls, cresols, caprolactam solution, epichlorohydrin, ethylene dichloride, glycols, hydrogen peroxide, isocyanates, ketones, maleic anhydride, nitrates, nitromethane, phenols, vinyl acetate. 

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