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ChemicalBook CAS DataBase List 3-Methoxybenzenethiol
15570-12-4

3-Methoxybenzenethiol synthesis

9synthesis methods
Taking m-bromoanisole as raw material, the organic magnesium compounds were firstly produced, then the Grignard reaction was carried out with solid sulfur, and finally 3-methoxybenzenethiol was produced by hydrolysis. The method is less polluting and easy
-

Yield:15570-12-4 89%

Reaction Conditions:

with sodiumsulfide nonahydrate;copper;ethane-1,2-dithiol in dimethyl sulfoxide at 100; for 20 h;Inert atmosphere;Green chemistry;

Steps:

General Experimental Procedure for the Synthesis of ArylThiols from Aryl Iodides
General procedure: To a test tube containing a magnetic bar was added aryl iodide(1 mmol), copper powder (6.35 mg, 0.1 mmol), Na2S·9H2O(720.54 mg, 3 mmol), and DMSO (2 mL). After flushing withargon, 1,2-ethanedithiol (8.4 μL, 0.1 mmol) was added. Themixture was stirred in the oil bath at 100 °C for 20 h. Aftercooled to ambient temperature, the reaction mixture was distributedin aq HCl (5%) and EtOAc. The organic layer was separated and washed with water and brine, dried, and concentratedunder vacuum. The crude product was further purifiedby column chromatography using ethyl acetate/n-hexane aseluent to provide the desired aryl thiol.

References:

Xue, Hongyu;Jing, Bing;Liu, Shasha;Chae, Junghyun;Liu, Yajun [Synlett,2017,vol. 28,# 17,art. no. ST-2017-W0384-L,p. 2272 - 2276]

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