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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7877생성일: 2026년 10월 23일

Hydrochloric Acid → 2-[2-(2-Ethyl-[1,3]dioxolan-2-yl)-ethyl]-5-methoxy-3-propyl-1-indanone

https://huagongshe.com/ko/reaction/7877

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium HydroxideHCID 14797—
반응물2-(2-Ethyl-1,3-dioxolan-2-yl)acetaldehydeHCID 13489223—
반응물5-Methoxy-3-propyl-1-indanoneHCID 21990859—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물2-[2-(2-Ethyl-[1,3]dioxolan-2-yl)-ethyl]-5-methoxy-3-propyl-1-indanoneHCID 2199085329.1%

반응 단계

A mixture of 5-methoxy-3-propyl-1-indanone (184 mg, 0.90 mmol) and (2-ethyl-[1,3]dioxolan-2-yl)acetaldehyde (173 mg, 1.20 mmol) was treated with a solution of KOH (85% wt. pure, 20 mg, 0.30 mmol) in ethanol (1.0 mL). The resulting mixture was stirred at room temperature for 30 minutes, then treated with 10% Pd on carbon (9 mg), placed under a hydrogen atmosphere, and stirred vigorously at room temperature for 18 hours. The mixture was acidified with 2N HCl and partitioned between EtOAc (9 mL) and water (5 mL). The organic phase was washed with brine, dried over MgSO4, filtered, and evaporated under vacuum to an oil (316 mg). The crude product was purified by chromatography on a Biotage FLASH 12M column, eluting with 10% EtOAc in hexanes, to afford 2-[2-(2-ethyl-[1,3]dioxolan-2-yl)-ethyl]-5-methoxy-3-propyl-1-indanone (87 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-61d811177b4e4cd88b1e29266c8ae876
출처 메모uspto-grants-2006_08