1,2-Dimercapto (CAS NO.: ), which is also known as o-Benzenedithiol, could be produced through the following synthetic routes.

A 200-ml. two-necked flask is fitted with an efficient Dry Ice-isopropyl alcohol condenser connected to a soda-lime tube, a magnetic stirrer, and a gas inlet tube. Isopropyl alcohol and Dry Ice are added to the condenser while the flask and condenser are flushed with dry nitrogen. The flask is immersed in a Dry Ice-isopropyl alcohol bath, and a vigorous stream of dry ammonia is introduced into the system. When about 80 ml. of liquid ammonia is condensed, the gas inlet tube is replaced with a ground-glass stopper. The cooling bath is removed, stirring is started, and 5.1 g. (0.020 mole) of 1,2-bis(n-butylthio) benzene is quickly introduced.

is now added in small pieces; the solution is allowed to decolorize before each successive piece is added. A water bath is placed occasionally under the flask to ensure continuous ebullition of ammonia. The blue color will persist for at least 15 minutes after 1.6 g. (0.070 g. atom) of sodium has been added. The excess sodium is then destroyed by cautious addition of 6 g. (0.11 mole) of ammonium chloride, with stirring. Cooling and stirring are stopped, and a slow stream of argon is passed in for a period of about 12–15 hours. The white solid residue is transferred to a beaker, and 300 g. of ice water is added, together with sufficient pellets of sodium hydroxide to make the solution alkaline. The alkaline solution is then extracted twice with ether and the ether extracts discarded. The solution is then acidified to with cold 1:1 (by volume) hydrochloric acid and extracted three times with ether. The ether extracts are combined, washed with water, and dried over anhydrous sodium sulfate. The ether is evaporated and the 1,2-dimercaptobenzene is distilled under reduced pressure under an atmosphere of nitrogen, giving a product which boils at 95°/5 mm. and usually solidifies after distillation. The yield is 1.6–2.4 g. (56–85%).