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HRID 36794作成日:2026年10月25日

Acetic Acid → Ethanesulfonamide, N-(3-amino-4-fluorophenyl)-

https://huagongshe.com/reaction/36794

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物N-(4-fluoro-3-nitrophenyl)ethanesulfonamideHCID 3286362—
触媒IronHCID 23925—
溶媒Ethyl AcetateHCID 8857—
生成物Ethanesulfonamide, N-(3-amino-4-fluorophenyl)-HCID 1113858489.2%

反応条件

温度80 °C

反応手順

A mixture of 63.1 g (1.13 mol) of iron powder and 120 ml of an aqueous solution of 5% acetic acid was heated to 80° C., and a mixed solution of 28.0 g (0.113 mol) of N-(4-fluoro-3-nitrophenyl)ethanesulfonamide, 116 ml of acetic acid and 116 ml of ethyl acetate was slowly added dropwise to the resultant mixture. After the reaction was continued for 3 hours, the insolubles were filtered out and washed with ethyl acetate. Thereafter the filtrate was distilled to remove the solvent, and the product was dissolved in ethyl acetate and washed with saturated sodium hydrogencarbonate, water and 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 22.0 g of the objective product (yield: 89%) in the form of light yellow crystals.

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-6f276f634d2f46a2b1429470c17ef2e6
出典メモuspto-grants-1995_05