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HRID 36793作成日:2026年10月25日

Ethanesulfonyl chloride → N-(4-fluoro-3-nitrophenyl)ethanesulfonamide

https://huagongshe.com/reaction/36793

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanesulfonyl chlorideHCID 11667—
反応物4-Fluoro-3-nitroanilineHCID 67768—
溶媒PyridineHCID 1049—
生成物N-(4-fluoro-3-nitrophenyl)ethanesulfonamideHCID 328636293%

反応手順

20.2 g (0.129 mol) of 4-fluoro-3-nitroaniline was dissolved in 120 ml of pyridine, and 17.8 g (0.136 mol) of ethanesulfonyl chloride was added dropwise to the solution at a temperature of not higher than 5° C. Thereafter the temperature was raised to room temperature and the reaction was continued for one night. After the pyridine was distilled off, the thus-obtained product was dissolved in ethyl acetate and washed with diluted hydrochloric acid twice, then with water, and with saturated saline solution. The solution was dried over anhydrous sodium sulfate, and the ethyl acetate was distilled off to obtain the crude product (crystals). The crude product was washed with diisopropyl ether, thereby obtaining 29.7 g of the objective product (yield: 93%) in the form of brown crystals. Melting point: 133° to 136° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05416236
出典データセットuspto-grants-1995_05
ORD IDord-0de8c25ef53b4f38b1dc4201c18a173f
出典メモuspto-grants-1995_05