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HRID 277000作成日:2026年10月25日

Bromine → 5-Bromo-3,3-diethyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/277000

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物Sodium AcetateHCID 517045—
反応物3,3-diethyl-2,3-dihydro-1H-indol-2-oneHCID 15153221—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物5-Bromo-3,3-diethyl-1,3-dihydro-2H-indol-2-oneHCID 21986250—

反応手順

A solution of 3,3-diethylindol-2-one (8 g, 40 mmol) and sodium acetate (4 g, 48 mmol) in acetic acid (100 ml) was treated with bromine (6.4 g, 40 mmol). After 30 min. the mixture was diluted with water and extracted with EtOAc (2×); the combined organic layers were washed with water, sat. sodium hydrogen carbonate solution, then brine, dried (MgSO4) and evaporated to afford the crude product (7.6 g, 75%). A sample was recrystallized from EtOAc/hexane to obtain 5-bromo-1,3-dihydro-3,3-diethyl-[2H]-indol-2-one, m. p. 164-165° C.; 1H-NMR (DMSO-d6) δ 10.45 (s, 1H), 7.41-7.40(d, 1H, J=2.2 Hz), 7.34-7.31 (m, 1H), 6.78-6.76 (d, 1H, J=8.2 Hz), 1.78-1.65 (m, 4H), 0.50-0.46 (m, 6H); MS (-ESI) m/z 266/268 (M−H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355648B1
出典データセットuspto-grants-2002_03
ORD IDord-ed1ba6631a054e9c8ebf9aa588c7baa7
出典メモuspto-grants-2002_03