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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1525739생성일: 2026년 10월 26일

Phenethyl bromide → 6-(2-Phenylethoxy)-1,2,3,4-tetrahydronaphthalen-1-one

https://huagongshe.com/reaction/1525739

반응식

참여 물질

역할이름HCID투입량
반응물Phenethyl bromideHCID 7666—
반응물Potassium CarbonateHCID 11430—
반응물6-Hydroxy-3,4-dihydro-1(2H)-naphthalenoneHCID 4679494—
용매AcetonitrileHCID 6342—
생성물6-(2-Phenylethoxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 1306733161.1%

반응 단계

To a solution of 6-hydroxy-3,4-dihydro-1(2H)-naphthalenone (2.0 g, 12.3 mmol) and (2-bromoethyl)benzene (4.8 g, 25.8 mmol) in ACN (20 mL) was added potassium carbonate (3.4 g, 24.6 mmol) at rt. The solution was heated at reflux overnight. The reaction was filtered, concentrated, and purified by silica gel chromatography (PE/EtOAc/DCM=10:1:2) to give 2.0 g (61%) of the title compound as a brown oil. 1H NMR (300 MHz, CDCl3): δ 2.08-2.16 (2H, m), 2.62 (2H, t, J=6.3 Hz), 2.92 (2H, t, J=6.3 Hz), 3.13 (2H, t, J=7.2 Hz), 2.92 (2H, t, J=7.2 Hz), 6.71 (1H, d, J=2.1 Hz), 6.83 (1H, dd, J=2.4, 8.7 Hz), 7.27-7.38 (5H, m), 8.01 (1H, dd, J=8.7 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09085534B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-c0b1650d827a489ab5731ed42abc7ca4
출처 메모uspto-grants-2015_07