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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29247생성일: 2026년 10월 24일

Formaldehyde → 2-Hydroxy-4-iodobenzaldehyde

https://huagongshe.com/ko/reaction/29247

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물TriethylamineHCID 8471—
반응물3-IodophenolHCID 12272—
반응물Ammonium ChlorideHCID 25517—
반응물Magnesium ChlorideHCID 5360315—
용매AcetonitrileHCID 6342—
생성물2-Hydroxy-4-iodobenzaldehydeHCID 18351513160.1%

반응 단계

To a solution of 3-iodophenol (3.00 g, 13.6 mmol) in acetonitrile (50 mL) was added magnesium chloride (3.89 g, 40.9 mmol), triethylamine (7.6 mL, 55 mmol), and paraformaldehyde (1.64 g, 55 mmol). The reaction mixture was refluxed overnight, then neutralized with saturated aqueous ammonium chloride. The resultant red precipitate was removed by filtration, and the filtrate was extracted with ethyl acetate. The precipitate was dissolved in methanol and added to the combined organic extracts, which were then dried over magnesium sulfate. The solvent was removed under reduced pressure to provide an orange solid (5.4 g) as the crude product. This material was used in the subsequent step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420066B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-02721cc0f01345be9e12390ff0c5239e
출처 메모uspto-grants-2008_09