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HRID 585685생성일: 2026년 10월 24일

Hydrochloric Acid → 4-(2,4-Dihydroxyphenyl)cyclohexanone

https://huagongshe.com/ko/reaction/585685

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물8-[2,4-Bis(methoxymethoxy)phenyl]-1,4-dioxaspiro[4.5]decaneHCID 12135169—
용매MethanolHCID 887—
생성물4-(2,4-Dihydroxyphenyl)cyclohexanoneHCID 994248968%

반응 단계

A round bottomed flask equipped with magnetic stirrer was loaded 8-[2,4-bis(methoxymethoxy)phenyl]-1,4-dioxaspiro[4.5]decane (1.30 g, 3.9 mmol) and methanol (15 ml). To the resulting stirred solution was added aqueous HCl (15 ml, 1M) in one portion. After stirring for one hr at room temperature the acid was quenched by adding saturated aqueous sodium bicarbonate solution (10 ml). After stirring vigorously for 10 min, the reaction mixture was transferred to a separating funnel and the phases separated and the aqueous phase was extracted with ethyl acetate (3×20 ml). The combined organic phases were washed with brine and the solvent evaporated. To the slightly wet crude product was added methanol (30 ml) and acidic ion exchange resin (4 g). The resulting mixture was heated under reflux, with stirring, for 5 hr. Filtering through a plug of Celite, washing with ethyl acetate, followed by removal of solvent in vacuo afforded an orange oil. Purification by flash column chromatography, (SiO2, ethyl acetate/petroleum ether, 1:1, v/v) furnished the title compound as a white powder (0.54 g, 68%). m/z (ES−) 411 (2M−1); δH (CD3OD) 1.94 (2H, ddd), 2.16-2.23 (2H, m), 2.41 (2H, dt), 2.62 (1H, t), 2.63 (1H, t), 6.24 (1H, dd), 6.31 (1H, d), 6.92 (1H, d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06933319B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-fcd04468a40f4e9abc134d51f3acbf4e
출처 메모uspto-grants-2005_08