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HRID 2165526作成日:2026年10月27日

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

https://huagongshe.com/reaction/2165526

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chlorideHCID 7369—
反応物Potassium CarbonateHCID 11430—
反応物2(1H)-Quinoxalinone, 3,4-dihydro-HCID 185949—
溶媒AcetoneHCID 180—
生成物4-(Benzenesulfonyl)-1,3-dihydroquinoxalin-2-oneHCID 109323752%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04940708
出典データセットuspto-grants-1990_07
ORD IDord-e63bd5bf0967443388cb193dc309b8b9
出典メモuspto-grants-1990_07