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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5389생성일: 2026년 10월 23일

Cyclooctanone → Ethyl 2-oxocyclononanecarboxylate

https://huagongshe.com/ko/reaction/5389

반응식

참여 물질

역할이름HCID투입량
반응물CyclooctanoneHCID 10403—
반응물Ethyl diazoacetateHCID 12192—
반응물Triethyloxonium tetrafluoroborateHCID 2723982—
용매DichloromethaneHCID 6344—
생성물Ethyl 2-oxocyclononanecarboxylateHCID 107210—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244889
출처 데이터셋uspto-grants-1993_09
ORD IDord-e3905ec671db4476912df221b80d4a05
출처 메모uspto-grants-1993_09