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HRID 418064作成日:2026年10月26日

Cesium carbonate → 3-Iodo-5-methanesulfonyl-phenol

https://huagongshe.com/reaction/418064

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Syn-benzaldehyde oximeHCID 5324470—
反応物1-Iodo-3-(methanesulfonyl)-5-nitrobenzeneHCID 57863042—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物3-Iodo-5-methanesulfonyl-phenolHCID 5786302455%

反応条件

温度90 °C

反応手順

To a solution of syn-benzaldehyde oxime (3.71 g, 30.6 mmol) in DMF (80 mL) was added cesium carbonate (19.9 g, 61.3 mmol) and heated to 90° C. for 1-2 min before a solution of 1-iodo-3-methanesulfonyl-5-nitro-benzene (5.0 g, 15.3 mmol) in DMF (80 mL) was added. The resulting dark brown solution was stirred at 90° C. for 15 h. The reaction mixture was then cooled down and diluted with EtOAc and washed with 10% HCl. The organic phase was then washed again with brine. The combined organic extracts were dried over sodium sulfate and evaporated under reduced pressure to obtain a crude brown oil which was purified on ISCO column (330 g). The desired compound was eluted with 70% EtOAc-Hexanes. The desired fractions were combined and evaporated under reduced pressure to afford 2.5 g (55%) of 3-iodo-5-methanesulfonyl-phenol as an orange solid. HR-ES(+) m/e calcd for C7H7O3SI (M+H)+ 298.9234, found 298.9234.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093253B2
出典データセットuspto-grants-2012_01
ORD IDord-1cb235526fba460f86844677a2254a6e
出典メモuspto-grants-2012_01