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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2165526생성일: 2026년 10월 26일

Benzenesulfonyl chloride → 4-(Benzenesulfonyl)-1,3-dihydroquinoxalin-2-one

https://huagongshe.com/reaction/2165526

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Potassium CarbonateHCID 11430—
반응물2(1H)-Quinoxalinone, 3,4-dihydro-HCID 185949—
용매AcetoneHCID 180—
생성물4-(Benzenesulfonyl)-1,3-dihydroquinoxalin-2-oneHCID 109323752%

반응 단계

A suspension of 10 g. (0.068 mole) of 3,4-dihydro-2(1H)-quinoxalinone (3,4-dihydro-2-hydroxyquinoxaline) [prepared in 50% yield according to the procedure described by W. H. Perkin et al. in the Journal of the Chemical Society, Vol. 123, p.2399(1923)] and 9.6 g. (0.069 mole) of potassium carbonate in 250 ml. of acetone was stirred under a nitrogen atmosphere at 40° C., while 11.5 g. (0.07 mole) of benzenesulfonyl chloride was added during the course of a 30-minute period. The reaction mixture was next heated at reflux temperature for 14 hours and then poured onto 500 ml. of ice. The resulting brown solid was recrystallized from ethyl acetate to yield 10.2 g (52%) of pure 4-benzenesulfonyl-3,4-dihydro-2(1H)-quinoxalinone, m.p. 183°-185° C. The pure product was further characterized by means of nuclear magnetic resonance data and elemental analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04940708
출처 데이터셋uspto-grants-1990_07
ORD IDord-e63bd5bf0967443388cb193dc309b8b9
출처 메모uspto-grants-1990_07