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HRID 859673作成日:2026年10月26日

Methanesulfonyl chloride → N-(4-bromo-2-ethylphenyl)methanesulfonamide

https://huagongshe.com/reaction/859673

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4-Bromo-2-ethylanilineHCID 2801283—
溶媒PyridineHCID 1049—
溶媒Ethyl AcetateHCID 8857—
生成物N-(4-bromo-2-ethylphenyl)methanesulfonamideHCID 646915281%

反応手順

4-Bromo-2-ethyl-aniline (2 mL, 14 mmol) dissolved in anhydrous pyridine (35 mL) at toom temperature was treated with methylsulfonyl chloride (1.3 mL, 16.8 mmol). The reaction was stirred at that temperature for 15 hours before it was diluted with EtOAc. The mixture was washed with H2O, brine and dried over MgSO4. The solvent was removed in vacuo and the residue was purified with flash chromatography (SiO2, 5–30% EtOAc in hexanes) to afford the desired product (3.1 g, 81% yield). 1H NMR (300 MHz, CDCl3): δ 1.25 (t, J=7.5 Hz, 3 H), 2.61–2.68 (m, 2 H), 3.02 (s, 3 H), 6.36 (s, 1 H), 7.36–7.39 (m, 3 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07151105B2
出典データセットuspto-grants-2006_12
ORD IDord-389a00c858154614be5cd1adf398aead
出典メモuspto-grants-2006_12