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HRID 1530125作成日:2026年10月26日

Bromine → Ethyl 2-bromo-3-(2,4-dichlorophenyl)-3-oxopropanoate

https://huagongshe.com/reaction/1530125

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物Ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoateHCID 542007—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 2-bromo-3-(2,4-dichlorophenyl)-3-oxopropanoateHCID 58094874—

反応手順

To a solution of ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate (3.95 g, 15.1 mmol) in dichloromethane (150 mL) was added a solution of bromine (0.935 mL, 18.2 mmol) in dichloromethane (20.0 mL) dropwise at 0° C. The solution was then stirred at room temperature for 1 hour. The reaction was quenched with 10% aqueous potassium carbonate solution, and then the layers were separated. The organic extracts were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude oil was used directly in the next step (5.27 g, quantitative). LCMS: (AA) ES+, 341. 1H NMR (400 MHz, d1-chloroform) (2 sets of signals, keto and enol): 12.78 (s, 1H), 7.73-7.28 (m, 2 sets of 3H), 5.73 (s, 1H), 4.37 (q, J=7.28 Hz, 2H), 4.29 (q, J=7.28 Hz, 2H), 1.41 (t, J=7.03 Hz, 3H), 1.29 (t, J=7.03 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09090601B2
出典データセットuspto-grants-2015_07
ORD IDord-612a2cca36e943c99dc11432f8128fa8
出典メモuspto-grants-2015_07