돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512581생성일: 2026년 10월 24일

Hydrochloric Acid → 4-[4-(6-Choroquinoxalin-2-yloxy)-2-ethylphenyl]-2,2,6,6-tetramethylpyran-3,5-dione

https://huagongshe.com/ko/reaction/512581

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물2,6-DichloroquinoxalineHCID 87748—
반응물4-(2-Ethyl-4-hydroxyphenyl)-2,2,6,6-tetramethylpyran-3,5-dioneHCID 66677553—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4-[4-(6-Choroquinoxalin-2-yloxy)-2-ethylphenyl]-2,2,6,6-tetramethylpyran-3,5-dioneHCID 66677663—

반응 조건

온도140 °C

반응 단계

4-(2-Ethyl-4-hydroxyphenyl)-2,2,6,6-tetramethylpyran-3,5-dione (0.100 g, 0.34 mmol) is added to a mixture of 2,6-dichloroquinoxaline (0.081 g, 0.41 mmol) and potassium carbonate (0.110 g, 0.69 mmol) in N,N-dimethylformamide (3 ml), and the mixture is heated at 140° C. under microwave irradiation for 40 minutes. The mixture is cooled to room temperature, then acidified by addition of 2M aqueous hydrochloric acid. The mixture is diluted with dichloromethane and passed through a phase separation cartridge. The organic phase is concentrated to around 2 ml, and purified by preparative reverse phase HPLC to give 4-[4-(6-choroquinoxalin-2-yloxy)-2-ethylphenyl]-2,2,6,6-tetramethylpyran-3,5-dione.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102642B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-75f355bd9e814310a9340f5d78597102
출처 메모uspto-grants-2015_08