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HRID 46800作成日:2026年10月25日

Dimethyl Sulfoxide → 4-Nitro-6-(trifluoromethyl)-2H-1,3-benzodithiol-2-one

https://huagongshe.com/reaction/46800

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物WaterHCID 962—
反応物4-Chloro-3,5-dinitrobenzotrifluorideHCID 9809—
反応物Sodium dimethyldithiocarbamic acidHCID 24189202—
溶媒ChloroformHCID 6212—
生成物4-Nitro-6-(trifluoromethyl)-2H-1,3-benzodithiol-2-oneHCID 1236111043.3%

反応手順

The compound of Example I is prepared in the following manner: To a magnetically stirred solution of 16.2 g (60 mmoles) 2,6-dinitro-4-trifluoromethylchlorobenzene in 60 ml. dimethylsulfoxide was added dropwise a solution of 10.74 g (60 mmoles) sodium dimethyldithiocarbamic acid. The reaction is mildly exothermic and accompanied by evolution of oxides of nitrogen. After allowing the reaction mixture to stir for 3 hours, 450 ml. water and 225 ml. chloroform are added and, after shaking well in an extraction funnel, the chloroform extract was withdrawn and the aqueous phase similarly extracted with two more 220 ml. portions of chloroform. The combined chloroform extract was washed thrice with 750 ml. portions of water, and dried over anhy. Na2SO4. After removing the solvent on a rotary evaporator, the residue was chromatographed over 180 g Silica-Gel. Elution with hexane-benzene (1:1) yielded 7.3 g (43.3%) 4-nitro-6-trifluoromethyl-1,3-benzodithiole-2-one, m.p. 103°-107° C. One recrystallization from ethanol yielded product, m.p. 111°-112° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04175186
出典データセットuspto-grants-1979_11
ORD IDord-136e956ca48f4a4d83b681b4519b042c
出典メモuspto-grants-1979_11