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HRID 990637作成日:2026年10月26日

Sodium Carbonate → 5-Bromo-3-methyl-indol-2-one

https://huagongshe.com/reaction/990637

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物BromineHCID 24408—
反応物3-MethyloxindoleHCID 150923—
反応物Sodium AcetateHCID 517045—
溶媒Acetic AcidHCID 176—
生成物5-Bromo-3-methyl-indol-2-oneHCID 2201937693.7%

反応手順

Under an atmosphere of nitrogen, bromine (0.96 g, 6.0 mmol) in acetic acid (5 cm3). was added drop wise to a solution of 3-methyl-2-indolinone (0.8749 g, 6.0 mmol) (Kende, et al, Synth. Commun., 12, 1, 1982) and sodium acetate (0.50 g, 6.0 mmol) in acetic acid (10 cm3). The reaction was stirred at room temperature for 3.5 h. Saturated sodium carbonate was added to quench the reaction. The water layer was extracted EtOAc (×3), dried (MgSO4), filtered, and evaporated to give the title compound (1.26 g, 93%), Mp=119-120° C.; 1H NMR (DMSO) δ 1.32 (d, 3H, J=7.66 Hz), 3.45 (q, 1H, J=7.62 Hz), 6.77 (d, 1H, J=8.23 Hz), 7.46 (s, 1H), 7.36-7.33 (m, 1H), 10.4 (s, 1H); IR (KBr) 3200, 1725 cm−1; MS (EI) m/z 224/226 (M−H)−; CHN calculated for C9H8BrNO: C, 47.82; H, 3.57; N, 6.20; Found: C, 47.44; H, 3.42; N, 6.04.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06462032B1
出典データセットuspto-grants-2002_10
ORD IDord-502dabb16e32404ebd2739f1cd3b52a5
出典メモuspto-grants-2002_10