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对位上具有不同取代基团的芳某丙烯基醚加溴生成相应的芳基、2,3-二溴丙基醚。这些新化合物与硫化氫鉀(或鈉)作用,其中对甲基、对溴及对氨基苯基、2,3-二溴丙基醚形成相应的2,3-二巯基丙基醚;对羧基化合物在冷甲醇液中也可形成二巯基化合物,但在冷水溶液中不起作用,热水溶液中則醚鍵發生水解,不能生成二巯基丙基醚;对硝基及对磺酰氨基化合物在甲醇液中冷时作用醚鍵也遭致水解。制得的四种二巯基丙醚与三氯化銻作用,并再將氯原子水解为羟基,生成相应的4-芳氧甲某-4,5-二氫-2-羟基-1,3-二間硫銻杂茂(4-Aryloxymethyl-4,5-dihydro-2-hydroxy-1,3-dithiastibiol)。
Brominated aromatic propenyl ethers with different substituent groups on the positions add bromine to the corresponding aryl groups, 2,3-dibromopropyl ether. These new compounds interact with potassium hydrogen sulphide (or sodium), in which the corresponding 2,3-dimercaptopropyl ethers are formed with 2,3-dibromopropyl ether for methyl, para-bromo and para-aminophenyl, Compounds can also form dimercapto compounds in cold methanolic solutions, but they do not work in cold aqueous solutions. Hydrolysis of ether bonds in hot aqueous solutions does not produce dimercaptopropyl ethers; the conversion of p-nitro and p-sulfonamido compounds in methanol Liquid ether role in the role of cold also suffered from hydrolysis. The four dimercaptopropyl ethers obtained reacted with antimony trichloride and then hydrolyzed the chlorine atom to the hydroxyl group to form the corresponding 4-aryloxymethylene-4,5-dihydro-2-hydroxy-1,3 4-Aryloxymethyl-4,5-dihydro-2-hydroxy-1,3-dithiastibiol.