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HRID 6872作成日:2026年10月24日

Sodium Carbonate → N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamide

https://huagongshe.com/ja/reaction/6872

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9-Borabicyclo(3.3.1)nonaneHCID 78966—
反応物4,4-Diethoxybut-1-eneHCID 256426—
反応物3-Bromo-N-cyclopropyl-4-fluorobenzamideHCID 22019090—
触媒HCID 178418397HCID 178418397—
溶媒BenzeneHCID 241—
溶媒EthanolHCID 702—
溶媒Ethyl AcetateHCID 8857—
生成物N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamideHCID 2201916393.4%

反応条件

温度80 °C

反応手順

A solution of 3-butenal diethyl acetal (144 mg, 1 mmol) and 9-BBN (0.5 M in THF, 2.2 mL, 1.1 mmol) was stirred at RT for 1 h. The mixture was concentrated and to the residue were added benzene (2 mL), EtOH (1 mL), aqueous Na2CO3 solution (2M, 1 mL), 3-bromo-4-fluoro-N-cyclopropylbenzamide (127 mg, 0.5 mmol) and Pd(Ph3P)4 (40 mg). The resulting mixture was stirred at 80° C. for 2 h. The mixture was then cooled to RT and diluted with ethyl acetate (10 mL) and washed with water. The organic layer was separated and concentrated. The residue was purified by column chromatography (SiO2; EtOAc/hexane 1:3) to afford N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamide (151 mg, 93%). This material was dissolved in acetone (1 mL) and 3 N HCl solution (0.2 mL) and stirred at RT for 1 h. The mixture was neutralized with NaHCO3 solution and extracted with ethyl acetate (3×5 mL). The organic layer was dried and concentrated to afford N-cyclopropyl-4-fluoro-3-(4-oxo-butyl)-benzamide (110 mg, 94%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084160B2
出典データセットuspto-grants-2006_08
ORD IDord-b66a4138f5a24ea6bea939d006b10a7b
出典メモuspto-grants-2006_08