戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 47239作成日:2026年10月23日

Formaldehyde → HCID 68837732、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物3-MethoxypropylamineHCID 1672—
反応物(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
溶媒EthanolHCID 702—
溶媒ChloroformHCID 6212—
生成物HCID 68837732HCID 688377321%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699863B1
出典データセットuspto-grants-2004_03
ORD IDord-2582b8a8a0d6406f90a949840fafd6f9
出典メモuspto-grants-2004_03