돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7831생성일: 2026년 10월 23일

Butanal → 2-Butyl-5-methoxy-1-indanone

https://huagongshe.com/ko/reaction/7831

반응식

참여 물질

역할이름HCID투입량
반응물ButanalHCID 261—
반응물Hydrochloric AcidHCID 313—
반응물Potassium HydroxideHCID 14797—
반응물5-Methoxyindan-1-oneHCID 78787—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물2-Butyl-5-methoxy-1-indanoneHCID 1204575253.2%

반응 단계

A mixture of 5-methoxy-1-indanone (25.0 g, 154 mmol), 85% KOH (2.03 g, 30.8 mmol), 10% palladium on activated carbon (2 g), and ethanol (150 mL) was placed under a hydrogen atmosphere and stirred while butyraldehyde (16.7 mL, 185 mmol) was added over 2 minutes. The mixture warmed during the addition. The resulting mixture was hydrogenated at room temperature for 3 hours, then filtered to remove the catalyst. The filtrate was acidified with 2N HCl (15.4 mL, 30.8 mmol) and evaporated under vacuum. The residue was partitioned between EtOAc (500 mL) and water (500 mL). The organic phase was washed with water (500 mL) and brine (100 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (33.5 g). The crude product was purified by column chromatography on EM silica gel 60 (230-400 mesh, 670 g), eluting first with CH2Cl2 and then with 5% EtOAc in CH2Cl2, to afford 2-butyl-5-methoxy-1-indanone (17.9 g) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-81064133f67440459d71cf2f2f14c79e
출처 메모uspto-grants-2006_08