Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14499생성일: 2026년 10월 25일
Acetic Acid → 3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-4-oxo-4H-chromene-8-carbaldehyde
https://huagongshe.com/reaction/14499
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Hexamethylenetetramine | HCID 4101 | — |
| 반응물 | 3-(4-Chlorophenyl)-7-hydroxy-2-isopropyl-chromen-4-one | HCID 16202451 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-4-oxo-4H-chromene-8-carbaldehyde | HCID 86625608 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07732435B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-e03fad2a09ea4f109a4d38cc1e388195 |
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| 출처 메모 | uspto-grants-2010_06 |
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