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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 611176생성일: 2026년 10월 26일

Acetic Acid → 1-(2-ethylmethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one

https://huagongshe.com/reaction/611176

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물FormaldehydeHCID 712—
반응물N-MethylethylamineHCID 12219—
반응물1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-oneHCID 19600145—
생성물1-(2-ethylmethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-oneHCID 67584926—

반응 조건

온도100 °C

반응 단계

To a solution of 0.400 g (1.345 mmol) of 1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one in 20 ml of acetic acid, 0.14 ml (1.6 mmol) of N-Ethylmethylamine and 0.13 9 (1.6 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 1 hour. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with aqueous sodium hydroxide and extracted with dichloromethane 3 times. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=4/1) to yield the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05998433
출처 데이터셋uspto-grants-1999_12
ORD IDord-6b244c45fd7d4ddeab8e414b0545dfed
출처 메모uspto-grants-1999_12