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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1444976생성일: 2026년 10월 25일

Hydrochloric Acid → Ethyl (1-hydroxy-2,5-dimethyl-4-oxocyclohexa-2,5-dien-1-yl)acetate

https://huagongshe.com/reaction/1444976

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,5-Dimethyl-4-benzoquinoneHCID 8718—
반응물Ethyl AcetateHCID 8857—
반응물HCID 178472539HCID 178472539—
용매TetrahydrofuranHCID 8028—
생성물Ethyl (1-hydroxy-2,5-dimethyl-4-oxocyclohexa-2,5-dien-1-yl)acetateHCID 4509381587%

반응 단계

Under nitrogen atmosphere, 6 mL of THF was added to 1.22 g (2 mmol, 0.6 equivalent) of (BrZnCH2COOEt.THF)2. Under argon atmosphere, a solution of 0.45 g (3.33 mmol) of 2,5-dimethyl-p-benzoquinone in 3 mL of THF was added 15 dropwise while stirring at 0˜5° C. The mixture was stirred at 20˜25° C. for 1 hour. 5 mL of 1N hydrochloric acid was added dropwise at 20° C. or lower, followed by dilution with 25 mL of ethyl acetate. Then, the layers were separated. The organic layer was washed successively with 5 mL (×2) of 1N hydrochloric acid, 5 mL of water, 5 mL (×2) of an aqueous saturated sodium bicarbonate solution, and 5 mL (×2) of an aqueous saturated sodium chloride solution. After washing, the organic layer was dried with anhydrous magnesium sulfate. After concentration under reduced pressure, purification with silica gel column (developing solvent; ethyl acetate/n-hexane=1/3, 1/2) afforded 0.65 g of the desired product (yield 87%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07662974B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-e9d75dd7247046c88a67006c175db5be
출처 메모uspto-grants-2010_02