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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 420238생성일: 2026년 10월 27일

Hydrochloric Acid → Ethyl 2-(1-hydroxycyclohex-2-en-1-yl)acetate

https://huagongshe.com/reaction/420238

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물2-Cyclohexen-1-oneHCID 13594—
반응물HCID 178472539HCID 178472539—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-(1-hydroxycyclohex-2-en-1-yl)acetateHCID 56644387%

반응 단계

Under nitrogen atmosphere, 20 mL of ethyl acetate was added to 3.05 g (5 mmol, 1.0 equivalent) of (BrZnCH2COOEt.THF)2. Under argon atmosphere, a solution of 0.48 g (5 mmol) of 2-cyclohexen-1-one in 5 mL of ethyl acetate was added dropwise while stirring at 0˜5° C. The mixture was stirred at 0˜5° C. for 3 hours. 10 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 (×2) of an aqueous saturated sodium chloride solution, 10 mL (×2) of an aqueous saturated sodium bicarbonate solution, and 10 mL of an aqueous saturated sodium chloride solution. After washing, the organic layer was dried with anhydrous magnesium sulfate. Concentration under reduced pressure afforded 0.80 g of the desired product (yield 87%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093403B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-f231fe79055847a1b26a3b7c452af06a
출처 메모uspto-grants-2012_01