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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7828생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/7828

반응식

참여 물질

역할이름HCID투입량
반응물ButanalHCID 261—
반응물DiisopropylamineHCID 7912—
반응물PentaneHCID 8003—
반응물5-Methoxyindan-1-oneHCID 78787—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-Butylidene-5-methoxy-1-indanoneHCID 67402813—

반응 단계

A solution of diisopropylamine (0.227 mL, 1.62 mmol) in anhydrous tetrahydrofuran (THF, 15 mL) was placed under a nitrogen atmosphere, cooled in an ice bath, and stirred while a 2.0M solution of butyllithium in pentane (0.771 mL, 1.54 mmol) was added dropwise over 2 minutes. The solution was stirred at room temperature for 15 minutes, then cooled in a dry ice-acetone bath and treated dropwise over 3 minutes with a solution of 5-methoxy-1-indanone (250 mg, 1.54 mmol) in THF (2 mL). After stirring at −78° C. for 20 minutes, the reaction mixture was treated with butyraldehyde (0.167 mL, 1.85 mmol). After stirring an additional 26 minutes at −78° C., the reaction mixture was removed from the cooling bath and stirred at room temperature for 90 hours. The reaction mixture was treated with saturated aqueous NH4Cl solution (10 mL) and extracted with EtOAc (15 mL). The organic phase was washed with brine (25 ml), dried over MgSO4, filtered, and evaporated under vacuum to an oil (353 mg). The crude product was purified by silica gel chromatography on a Biotage FLASH 12M column (1.2×15 cm), eluting with 7:1 hexanes-EtOAc, to afford 2-butylidene-5-methoxy-1-indanone (205 mg) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-348e8a54c7c84684b360fbaec8b6e185
출처 메모uspto-grants-2006_08