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HRID 5389作成日:2026年10月25日

Cyclooctanone → Ethyl 2-oxocyclononanecarboxylate

https://huagongshe.com/reaction/5389

反応式

関与物質

役割名称HCID仕込み量
反応物CyclooctanoneHCID 10403—
反応物Ethyl diazoacetateHCID 12192—
反応物Triethyloxonium tetrafluoroborateHCID 2723982—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 2-oxocyclononanecarboxylateHCID 107210—

反応条件

温度0 °C

反応手順

Cyclooctanone (25 g, 198 mmol) is dissolved in methylene chloride (500 mL) and the solution is cooled to 0° C. Triethyloxonium tetrafluoroborate (121.6 g, 640 mmol) is added. Ethyl diazoacetate (41.61 g, 365 mmol) is then added dropwise over 25 minutes, and the reaction is stirred at 0° C. for 4 hours. The reaction is quenched by pouring into a solution of sodium bicarbonate (160 g) in water (1.6 L) and stirring overnight. The reaction mixture is then extracted several times with methylene chloride, the combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by vacuum distillation (0.2-1.0 mm Hg) and the fraction boiling between 100°-125° C. is collected to give 2-ethoxycarbonyl-cyclononanone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244889
出典データセットuspto-grants-1993_09
ORD IDord-e3905ec671db4476912df221b80d4a05
出典メモuspto-grants-1993_09