Identification | More | [Name]
Sodium 4-chlorobenzene sulfinate | [CAS]
14752-66-0 | [Synonyms]
4-CHLOROBENZENESULFINIC ACID SODIUM SALT 4-CHLOROBENZENESULFINIC ACID SODIUM SALT HYDRATE 4-CHLOROBENZENESULPHINIC ACID SODIUM SALT P-CHLOROBENZENESULFINIC ACID SODIUM SALT SODIUM 4-CHLOROBENZENESULFINATE SODIUM 4-CHLOROBENZENE SULFINIC ACID Benzenesulfinicacid,4-chloro-,sodiumsalt Sodium 4-chlorobenzenesulphinate sodium p-chlorobenzenesulphinate 4-Chlorobenzenesulfinic acid sodium salt, 97+% 4-Chlorobenzenesulfinic acid hydrate sodium salt Sodium 4-chlorobenzenesulfinate hydrate | [EINECS(EC#)]
238-811-9 | [Molecular Formula]
C6H4ClNaO2S | [MDL Number]
MFCD00035602 | [Molecular Weight]
198.6 | [MOL File]
14752-66-0.mol |
Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . S22:Do not breathe dust . | [PackingGroup ]
III | [HS Code ]
29309090 |
Hazard Information | Back Directory | [Chemical Properties]
white crystalline powder | [Synthesis]
The general procedure for the synthesis of sodium 4-chlorobenzenesulfinate from 4-chlorobenzenesulfonyl chloride: chlorobenzene (3.23 g, 28 mmol) was added dropwise to chlorosulfonic acid (10 g, 86 mmol) at a strictly controlled temperature not exceeding 20°C. The reaction was carried out by stirring for 1 hour. After completion of the reaction, the reaction solution was stirred at room temperature for 1 h, followed by slow pouring into ice (50 g) for quenching. The precipitate was collected by filtration, washed with water and added in batches to a solution of sodium bisulfite (7.5 g, 60 mmol) in water (28 mL). The mixture was heated to 90 °C and stirred for 1 h, during which a 50% sodium hydroxide solution was added slowly and dropwise to maintain the pH of the reaction system between 8-9. At the end of the reaction, the reaction mixture was filtered and the filtrate was allowed to stand at room temperature for 10 hours to crystallize. Filtration gave a white crystalline 4-chlorobenzenesulfinic acid sodium salt product, which was washed with cold water and dried at room temperature. The final product 3 was obtained in 75% yield (4.3 g). The characteristic absorption peaks (cm-1 ) of the IR spectrum of the product were as follows: 1575 (aromatic C-H stretching vibration); 1340, 1130 (SO2 symmetric and asymmetric stretching vibration); 1004, 981 (C-H in-plane bending vibration); 832, 740 (C-Cl stretching vibration). | [References]
[1] Tetrahedron Letters, 2014, vol. 55, # 29, p. 3851 - 3855 [2] Chemistry - An Asian Journal, 2016, vol. 11, # 15, p. 2121 - 2125 [3] Acta Chemica Scandinavica, Series A: Physical and Inorganic Chemistry, 1976, vol. A30, # 8, p. 579 - 585 [4] European Journal of Medicinal Chemistry, 2007, vol. 42, # 6, p. 880 - 884 [5] Patent: WO2007/66844, 2007, A1. Location in patent: Page/Page column 14-15 |
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