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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65090생성일: 2026년 10월 25일

2-(4-Methoxyphenoxy)ethylamine → Alpha-isopropyl-alpha-[3-[N-[2-(4-methoxyphenoxy)ethyl]amino]-propyl]-3,4-dimethoxyphenylacetonitrile

https://huagongshe.com/reaction/65090

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Methoxyphenoxy)ethylamineHCID 1797793—
반응물3-(3,4-Dimethoxyphenyl)-2-methyl-6-oxohexane-3-carbonitrileHCID 3015370—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
생성물Alpha-isopropyl-alpha-[3-[N-[2-(4-methoxyphenoxy)ethyl]amino]-propyl]-3,4-dimethoxyphenylacetonitrileHCID 1371471357.4%

반응 단계

A solution of 3.96 g of 4-cyano-4-isopropyl-4-(3,4-dimethoxyphenyl)butyraldehyde and 2.00 g of 2-(4-methoxyphenoxy)ethylamine in 50 ml of ethanol was refluxed for 1 hour. To the solution was added 0.55 g of sodium borohydride under ice-cooling, and the solution was stirred for 30 minutes at room temperature. The solvent was removed and the residue was dissolved in 10% hydrochloric acid and washed with ether. The aqueous layer was made alkaline with potassium carbonate and extracted with ethyl acetate. The extract was washed with water, dried, and evaporated. The residue was chromatographed on silica gel using chloroform as an eluent to give 2.93 g of the desired compound as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04612329
출처 데이터셋uspto-grants-1986_09
ORD IDord-8c07906cda044c0d91383a292b90ea13
출처 메모uspto-grants-1986_09