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HRID 461822생성일: 2026년 10월 25일

Sulfuric Acid → 6-chloro-5,7-dimethyl-4-oxo-4H-1-benzopyran-2-carboxylic acid

https://huagongshe.com/reaction/461822

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물4-Chloro-3,5-dimethylphenolHCID 2723—
반응물Dimethyl acetylenedicarboxylateHCID 12980—
반응물Sodium HydroxideHCID 14798—
반응물Benzyltrimethylammonium hydroxideHCID 66854—
용매MethanolHCID 887—
용매1,4-DioxaneHCID 31275—
생성물6-chloro-5,7-dimethyl-4-oxo-4H-1-benzopyran-2-carboxylic acidHCID 21392596—

반응 조건

온도0 °C

반응 단계

0.5 Parts of benzyl trimethylammonium hydroxide were added dropwise to a mixture of 156.6 parts of 4-chloro-3, 5-xylenol, 149.1 parts of dimethyl acetylene dicarboxylate and 30 parts of dioxan. The reaction mixture was heated for 1/2 hour on the steam bath, cooled, and basified with 320 parts of 25% aqueous sodium hydroxide solution. After addition of 100 parts of methanol the red solution was heated at reflux for 3 hours on the steam bath, cooled, and acidified with excess dilute sulphuric acid. The precipitated yellow solid was filtered, washed with a little water, and dried. The solid was added portionwise to 850 parts of stirred chlorosulphonic acid cooled to 0° C. When all the solid had dissolved, the dark red solution was added cautiously dropwise to excess ice-water. The precipitated solid was filtered, washed with water, and recrystallised from a dioxan aqueous ethanol mixture to give 157.1 parts of 6-chloro-5,7-dimethyl-4-oxo-4H-1-benzopyran-2-carboxylic acid as a colourless solid, melting point 289°-290° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04064256
출처 데이터셋uspto-grants-1977_12
ORD IDord-39b0c557d23b47318e7ee8c4f9597455
출처 메모uspto-grants-1977_12