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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662158생성일: 2026년 10월 27일

2-Cyclohexen-1-one → (R)-3-(4-(trifluoromethyl)phenyl)cyclohexanone

https://huagongshe.com/reaction/1662158

반응식

참여 물질

역할이름HCID투입량
반응물2-Cyclohexen-1-oneHCID 13594—
반응물4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
촉매ethene;(Z)-4-hydroxypent-3-en-2-one;rhodiumHCID 11010647—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물(R)-3-(4-(trifluoromethyl)phenyl)cyclohexanoneHCID 11436439—

반응 조건

온도100 °C

반응 단계

To a 40 ml microwave flask containing dioxane/H2O (10/1) (22 mL) was added cyclohexen-1-one (1.35 g, 14.0 mmol), acetylacetonatobis(ethylene)rhodium(I) (0.36 g, 1.40 mmol), R-2,2′-bis(diphenyl-phosphino)-1,1′-binaphthyl (0.88 g, 1.40 mmol) and 4-(trifluoromethyl)-phenylboronic acid (5.0 g, 28.0 mmol). The mixture was heated in the microwave (Personal Chemistry) at 100° C. for 20 minutes. The material was transferred to a separatory funnel and extracted with ethyl acetate (150 mL). The resulting organic layer was washed with NaHCO3 (75 mL), dried (Na2SO4), filtered and concentrated under reduced pressure. The mixture was purified on SiO2 (hexane/ethyl acetate 4/1) to provide the title compound. [α]D=+13.62 c=10 (CH3OH). 1H NMR (CD3OD, 300 MHz); δ 1.72-2.20 (m, 5H), 2.35-2.73 (m, 3H), 3.06-3.15 (m, 1H), 7.40-7.42 (m, 2H), 7.46-7.63 (m, 2H). MS (+ESI) m/z 242 (M+NH4—H2O)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08030504B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-1c06f8f3fb814c59911b62ca7dc8a1fd
출처 메모uspto-grants-2011_10