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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12611생성일: 2026년 10월 25일

Ethyl (2-oxo-cyclohex-3-enyl)acetate → Ethyl [4-(4-fluorophenyl)-2-oxo-cyclohexyl]acetate

https://huagongshe.com/reaction/12611

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl (2-oxo-cyclohex-3-enyl)acetateHCID 13834278—
반응물HCID 178418676HCID 178418676—
용매Dimethyl SulfideHCID 1068—
용매TetrahydrofuranHCID 8028—
생성물Ethyl [4-(4-fluorophenyl)-2-oxo-cyclohexyl]acetateHCID 91222586—

반응 단계

This ester (4 g, 0.022 mmol), copper (I) bromide-dimethyl sulfide complex (4.88 g, 0.023 mmol) in dimethyl sulfide (20 ml) and tetrahydrofuran (120 ml) was cooled to −40° C. under nitrogen and treated dropwise with 4-fluorophenylmagnesium bromide (1M solution in THF, 43.9 ml) so that the temperature did not rise above −40° C. Reaction was stirred for 20 minutes before quenching with 1N HCl (300 ml) and extracting the products with ether (3×300 ml). Combined organic phase washed with saturated sodium chloride, dried over magnesium sulfate and evaporated to dryness. The crude oil was purified by silica chromatography eluting with hexane-ethyl acetate mixtures (10-20%), to give ethyl [4-(4-fluorophenyl)-2-oxo-cyclohexyl]acetate as a colourless oil, 2.8 g. 1H NMR δ (ppm) (CDCl3): 7.26-7.11 (2H, m), 7.04-6.94 (2H, m), 4.18-4.11 (2H, m), 3.55-3.44 (1H, m), 3.00-2.90 (1H, m), 2.80-2.73 (2H, m), 2.69-2.55 (1H, m), 2.28-2.17 (2H, m), 2.10-1.88 (2H, m), 1.61-1.42 (1H, m) and 1.31-1.25 (3H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728022B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-2d4777b6081240f594287e9174a72b72
출처 메모uspto-grants-2010_06