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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1444964생성일: 2026년 10월 26일

Hydrochloric Acid → diethyl(2E)-4-hydroxy-4-phenylhex-2-enedioate

https://huagongshe.com/reaction/1444964

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물Ethyl (2E)-4-oxo-4-phenyl-2-butenoateHCID 5369605—
반응물HCID 178472539HCID 178472539—
용매TetrahydrofuranHCID 8028—
생성물diethyl(2E)-4-hydroxy-4-phenylhex-2-enedioateHCID 5746581497%

반응 단계

Under nitrogen atmosphere, 15 mL of THF was added to 3.05 g (5 mmol, 1.0 equivalent) of (BrZnCH2COOEt.THF)2. Under argon atmosphere, a solution of 1.02 g (5 mmol) of trans-ethyl 3-benzoylacrylate in 2.5 mL of THF was added dropwise while stirring at 0˜5° C. The mixture was stirred at 20˜25° C. for 3 hours. 7.5 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, 10 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. Concentration under reduced pressure afforded 1.42 g of the desired product (yield 97%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07662974B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-e70c798e2af1488e925577f9c4932857
출처 메모uspto-grants-2010_02