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HRID 39203作成日:2026年10月24日

Acetic Anhydride → N-(3-bromobenzenesulfonyl)acetamide

https://huagongshe.com/ja/reaction/39203

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物3-Bromobenzene-1-sulfonamideHCID 2734765—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒PyridineHCID 1049—
溶媒Ethyl AcetateHCID 8857—
生成物N-(3-bromobenzenesulfonyl)acetamideHCID 6121623351%

反応手順

3-Bromobenzenesulfonamide (470 mg, 2.0 mmol) was dissolved in pyridine (1 mL). To this solution was added DMAP (7.3 mg, 0.060 mmol) and then acetic anhydride (570 μL, 6.0 mmol). The reaction was stirred for 3 h at room temperature during which time the reaction changed from a yellow solution to a clear solution. The solution was diluted with ethyl acetate, and then washed with aqueous NH4Cl solution (×3) and water. The organic layer was dried over MgSO4 and concentrated. The resulting oil was triturated with hexanes and the precipitate was collected by filtration to obtain N-(3-bromophenylsulfonyl)-acetamide as a shiny white solid (280 mg, 51%). 1H NMR (400 MHz, DMSO-d6) δ 12.43 (s, 1H), 8.01 (t, J=1.8 Hz, 1H), 7.96-7.90 (m, 2H), 7.61 (t, J=8.0 Hz, 1H), 1.95 (s, 3H); HPLC ret. time 1.06 min; ESI-MS 278.1 m/z (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524767B2
出典データセットuspto-grants-2013_09
ORD IDord-63a2ec6c447d4e18a1ffe336ff4d2000
出典メモuspto-grants-2013_09