Abstract: Aryl alkyl ethers can be produced by the reaction of hydroxyaromatics with an alcohol in the presence of a catalyst. This process achieves higher yields of aryl alkyl ethers and the formation of ring-alkylated products and dialkyl ethers is markedly reduced.

Abstract: An arylamine such as aniline is condensed with formaldehyde in the presence of aqueous hydrochloric acid to form a mass containing the hydrogen chloride salt of a polyarylpolyamine. The mass is contacted with additional aniline thereby forming an organic phase and an aqueous phase, the 4,4'-polyarylpolyamine overwhelmingly being liberated from its salt form in the aqueous phase and being transferred to the organic phase. High recoveries of the 4,4'-diamino polycondensate are achieved.

Abstract: A process has been invented for the preparation of polyaryl polyamines having methylene bridges by condensation of primary arylamines with formaldehyde in the presence of a catalyst. According to the invention, the amount of binuclear compounds and an improved viscosity can be obtained if one adds the remaining amount of primary arylamine immediately after the formaldehyde.

Abstract: Through condensation ortho- and para-isomers of methylene dianiline (MDA) as well as PMPPA are produced as condensation products from arylamines, especially from aniline, and formaldehyde in the presence of acid catalysts, in which at least one component is a perfluoro-carbonic acid. From this mixture of the condensation products, 4,4'-MDA (p-isomer) of high purity is obtained by crystallization while the homogeneous aqueous solution obtained is being cooled down. It has been discovered that the 4,4'-MDA salts of the perfluoro-carbonic acids are less soluble in water than the corresponding salts of the o-isomers and the PMPPA.

Abstract: Hydroquinone is made by heating an aqueous solution of p-aminophenol, or of a salt of p-aminophenol with an acid made by catalytic or electrolytic reduction of nitrobenzene, with an organic sulfonic acid, and extracting from the reaction mixture the hydroquinone by contact with a water-insoluble solvent. Residual organic sulfonic acid can be recovered from the hydroquinone-free reaction mixture and reused.

Abstract: An arylamine such as aniline is condensed with formaldehyde in the presence of aqueous hydrochloric acid to form a mass containing the hydrogen chloride salt of a polyarylpolyamine. The mass is contacted with additional aniline thereby forming an organic phase and an aqueous phase, the 4,4'-polyarylpolyamine overwhelmingly being liberated from its salt form in the aqueous phase and being transferred to the organic phase. High recoveries of the 4,4'-diamino polycondensate are achieved.