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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47240생성일: 2026년 10월 24일

Formaldehyde → 1-Butylaminomethyl-3-(1H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one

https://huagongshe.com/ko/reaction/47240

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참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물ButylamineHCID 8007—
반응물HexaneHCID 8058—
반응물(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
용매EthanolHCID 702—
생성물1-Butylaminomethyl-3-(1H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-oneHCID 68834641—

반응 조건

온도0 °C

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 butylamine (56.4 μL, 0.571 mmol) in 5.5 mL of EtOH was heated at reflux for 2.5 h. Then reaction mixture was treated with 2 mL of hexane was and then cooled to 0° C. The reaction mixture was then filtered to remove Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one. The filtrate was partitioned between dilute HCl and ethyl acetate. The organic layer was removed and the aqueous layer washed with 15 mL Ethyl acetate. The aqueous phase 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 solvent was removed in vacuo to give 58 mg of yellow oil. The oil was purified by chromatography (silica gel, 1:1/hexane:ethyl acetate) to give the title compound (51.6 mg, 31%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699863B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-df79f2cf7a9b4263834f59cd3ebdf5e4
출처 메모uspto-grants-2004_03