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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 899생성일: 2026년 10월 23일

1,2-Cyclohexanedione → 4-Oxo-4,5,6,7-tetrahydro-1-benzofuran-3-carboxylic acid

https://huagongshe.com/ko/reaction/899

반응식

참여 물질

역할이름HCID투입량
반응물1,2-CyclohexanedioneHCID 13006—
반응물Potassium HydroxideHCID 14797—
반응물Sodium HydroxideHCID 14798—
반응물Ethyl bromopyruvateHCID 66144—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4-Oxo-4,5,6,7-tetrahydro-1-benzofuran-3-carboxylic acidHCID 713937—

반응 조건

온도0 °C

반응 단계

4-Oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid was prepared as follows: To a stirred solution of potassium hydroxide (28.06 g, 0.5 mol) in methyl alcohol (100 mL) under nitrogen at 0° C. was added dropwise a solution of cyclohexanedione (56.07 g, 0.5 mol) in methyl alcohol (100 mL). The mixture was stirred at 0° C. for 0.5 h, then a solution of ethyl bromopyruvate (66 mL, 0.525 mol) in methyl alcohol(100 mL) was added dropwise. After allowing the mixture to stir at ambient temperature for 17 h, a 50% aqueous sodium hydroxide solution (60 mL) was added dropwise and stirring continued an additional 7 h. After dilution with water, the solution was acidified and the methanol removed in vacuo. Ice water was added and the precipitate filtered and dried in vacuo to afford 4-oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid. m.p. 137°-138° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723462
출처 데이터셋uspto-grants-1998_03
ORD IDord-754d50c008364ac9b11186dee1fd24b1
출처 메모uspto-grants-1998_03