A thiophenol, C 6 H 5 SH, is known, and is prepared by the action of phosphorus pentasulphide on phenol, or by distilling a mixture of sodium benzene sulphonate and potassium sulphydrate.
The residue crystallizes slowly, and the crystalline product is almost wholly d-benzyl-allyl-phenyl-ammonium-d-sulphonate, the corresponding /-compound remaining as a syrupy residue.
A-Naphthol may be prepared by fusing sodium-a-naphthalene sulphonate with caustic soda; by heating a-naphthylamine sulphate with water to 200° C. (English Patent 14301 (1892)); and by heating phenyl isocrotonic acid (R.
0-Naphthol, C 1 oH 7 OH, prepared by fusing sodium 0-naphthalene sulphonate with caustic soda, crystallizes in plates which melt at 122° C. With ferric chloride it gives a green colouration, and after a time a white flocculent precipitate of a dinaphthol.
A-Naphthoic acid, C 1 oH 7 CO 2 H, is formed by hydrolysis of the nitrile, obtained by distilling potassiuma-naphthalene sulphonate with potassium cyanide (V.
Chemie, 1868, p. 34), or by heating the sulphonate with sodium formate (V.
Bokorny, moreover, it appears that such filaments will yield :starch from formaldehyde when they are supplied with sodium -oxymethyl sulphonate, a salt which readily decomposes into formaldehyde and hydrogen sodium sulphite, an observation which has been taken to mean that formaldehyde is always a stage in the synthesis of starch.
Lunge, Berichte, 1877, 10, p. 12 75); by fusing sodium benzene sulphonate with sodium formate: C6H5S03Na+-HC02Na=C6HS000Na+ NaHS0 3; by heating calcium phthalate with calcium hydroxide to 330 0 -350° C.; by heating benzotrichloride with water in a sealed tube, and from the hippuric acid which is found in the urine of the herbivorae.
Perkin; the method being to sulphonate anthraquinone, and then to convert the sulphonic acid into its sodium salt and fuse this with caustic soda.
Ten volumes of the purest coal-tar benzene were shaken for four hours with one volume of sulphuric acid, the acid layer was removed and neutralized with lead carbonate, and the lead thiophen sulphonate obtained was distilled with an equivalent quantity of ammonium chloride.