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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14499생성일: 2026년 10월 24일

Acetic Acid → 3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-4-oxo-4H-chromene-8-carbaldehyde

https://huagongshe.com/ko/reaction/14499

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물HexamethylenetetramineHCID 4101—
반응물3-(4-Chlorophenyl)-7-hydroxy-2-isopropyl-chromen-4-oneHCID 16202451—
용매DichloromethaneHCID 6344—
생성물3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-4-oxo-4H-chromene-8-carbaldehydeHCID 86625608—

반응 조건

온도100 °C

반응 단계

A mixture of 3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-chromen-4-one (12.48 g, 39.6 mmol) and hexamethylenetetramine (39.46 g, 0.28 mol) in acetic acid (250 ml) is stirred at 100° C. for 20 h. After the mixture has cooled to room temperature, the solvent is removed in vacuo to afford a black oily residue. 5M HCl solution (150 ml) is added, and the mixture is heated under reflux for 30 min. The reaction mixture is poured onto ice/water, and the resulting brown solid is isolated by filtration. The solid is taken up in dichloromethane, the mixture is passed through a bed of Celite, and the solvent is evaporated in vacuo. The solid residue is stirred at room temperature with ethyl acetate, filtered and washed with hexane to afford the desired product as a pale brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732435B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e03fad2a09ea4f109a4d38cc1e388195
출처 메모uspto-grants-2010_06