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HRID 839952作成日:2026年10月25日

Sodium Hydroxide → 2-(3,5-Dichlorobenzene-1-sulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazole

https://huagongshe.com/reaction/839952

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Sodium SulfiteHCID 24437—
反応物2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazoleHCID 12874685—
反応物3,5-DichlorobenzenesulfinateHCID 17950865—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(3,5-Dichlorobenzene-1-sulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazoleHCID 2032288370%

反応手順

A solution of 75.6 g (0.6 mole) of analytically pure sodium sulfite in 300 ml of water was pre-warmed to 60°-70° C in a beaker. 122.8 g (0.5 mole) of 3,5-dichlorobenzenesulfochloride, and a solution of 40 g (1 mole) of sodium hydroxide in 200 ml of water were synchronously added dropwise from two dropping funnels in such a way that the pH value (measured with an electrode in the reaction solution) was always between 7 and 9; during the addition the mixture was stirred magnetically. The saline solution of the 3,5-dichlorobenzenesulfinate (about 600 ml) was then diluted with 1.8 liters of dimethylformamide and after adding 116.5 g (0.5 mole) of 2-bromo-5-trifluoromethyl-1,3,4-thiadiazole the whole was stirred for 15 hours at 50° C. The sulfone was precipitated completely by adding ice water and was recrystallized from ethanol. 121 g (70% of theory) of 2-(3',5'-dichlorophenylsulfonyl)-5-trifluoromethyl-1,3,4-thiadiazole of melting point 123° C were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04097669
出典データセットuspto-grants-1978_06
ORD IDord-a03dd99102214b99ac881afb4d6bb399
出典メモuspto-grants-1978_06