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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47239생성일: 2026년 10월 23일

Formaldehyde → HCID 68837732, 화합물

https://huagongshe.com/ko/reaction/47239

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물3-MethoxypropylamineHCID 1672—
반응물(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
생성물HCID 68837732HCID 688377321%

반응 단계

A mixture of Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one (120.0 mg, 0.571 mmol), paraformaldehyde (17.1 mg, 0.571 mmol), and 3-methoxypropylamine (58.2 μL, 0.571 mmol) in 4.0 mL EtOH was heated at reflux for 6.5 h. The reaction mixture was cooled to room temperature and let stand for 22 h. The reaction mixture was filtered and the filter cake rinsed with 30% ethyl acetate in hexane. The filtrate was concentrated in vacuo and 4 ML of EtOH added. The reaction was refluxed an additional 19.5 h. The reaction mixture was cooled to room temperature and partitioned between 30 mL dilute HCl and 20 mL Ethyl acetate. The organic layer was removed and the aqueous layer washed with 15 mL ethyl acetate. The aqueous layer was made basic to pH 8 with saturated NaHCO3 and extracted with ethyl acetate. The ethyl acetate layer was washed with H2O, brine and dried over anhydrous Na2SO4. The ethyl acetate layer was filtered and then concentrated. The solid obtained (42.5 mg) was dissolved in CHCl3 and purified by chromatography (silica gel, 1:1/hexane:acetone) to give the title compound (1.5 mg, 1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699863B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-2582b8a8a0d6406f90a949840fafd6f9
출처 메모uspto-grants-2004_03