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HRID 505671作成日:2026年10月26日

Methanesulfonyl chloride → N-[2-bromo-5-(trifluoromethyl)phenyl]methanesulfonamide

https://huagongshe.com/reaction/505671

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonyl chlorideHCID 31297—
反応物2-Bromo-5-(trifluoromethyl)benzenamineHCID 67989—
溶媒PyridineHCID 1049—
生成物N-[2-bromo-5-(trifluoromethyl)phenyl]methanesulfonamideHCID 5943090452%

反応手順

To a solution of 2-bromo-5-trifluoromethylaniline (3.18 g, 13.25 mmol) in pyridine (18 ml) was added methanesulfonyl chloride (1.03 ml, 13.25 mmol) and the mixture was stirred for 6 hours at room temperature. The solvent was removed in vacuo and the residue was diluted with chloroform. The organic layer was washed with water, 1N hydrochloric acid, a saturated sodium hydrogen carbonate solution and saturated brine and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by recrystallization to give the subject compound (2.18 g, 52%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07781479B2
出典データセットuspto-grants-2010_08
ORD IDord-5888ddb31d474185be9e29694440c5d9
出典メモuspto-grants-2010_08